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The development of efficient catalysts is a highly necessary but challenging task within the field of environmental water remediation. Single-atom catalysts are promising nanomaterials within this respect, but in-depth studies encompassing this class of catalysts remain elusive. In this work, we systematically study the degradation of gemfibrozil, a persistent pollutant, on a series of carbon nitride photocatalysts, investigating both the effect of (i) catalyst textural properties and (ii) metal single atoms on the contaminant degradation. Tests in the absence of the catalyst result in negligible degradation rates, confirming the stability of the contaminant when dispersed in water. Then, photocatalytic tests at optimal pH, solvent, and wavelength reveal a correlation between the support surface area and the degradation. This points to the role of carbon nitride surface nanostructure on gemfibrozil degradation. In particular, the use of silver on mesoporous carbon nitride single-atom catalyst (Ag@mpgC

Semiconductor photocatalysis is a potential pathway to solve the problems of global energy shortage and environmental pollution. Black phosphorus (BP) has been widely used in the field of photocatalysis owing to its features of high hole mobility, adjustable bandgap, and wide optical absorption range. Nevertheless, pristine BP still exhibits unsatisfactory photocatalytic activity due to the low separation efficiency of photoinduced charge carriers. In recent years, the construction of heterostructured photocatalysts based on BP has become a research hotspot in photocatalysis with the remarkable improvement of photoexcited charge-separation efficiency. Herein, progress on the design, synthesis, properties, and applications of BP and its corresponding heterostructured photocatalysts is summarized. Furthermore, the photocatalytic applications of BP-based heterostructured photocatalysts in water splitting, pollutant degradation, carbon dioxide reduction, nitrogen fixation, bacterial disinfection, and organic synthesis are reviewed. Opportunities and challenges for the exploration of advanced BP-based heterostructured photocatalysts are presented. This review will promote the development and applications of BP-based heterostructured photocatalysts in energy conversion and environmental remediation.

Natural waters, water droplets in the air at coastal regions and wastewaters usually contain chloride ions (Cl-) in relatively high concentrations in the milimolar range. In the reactions of highly oxidizing radicals (e.g.,•OH,•NO3, or SO4•-) in the nature or during wastewater treatment in advanced oxidation processes the chloride ions easily transform to chlorine containing radicals, such as Cl•, Cl2•-, and ClO•. This transformation basically affects the degradation of organic molecules. In this review about 400 rate constants of the dichloride radical anion (Cl2•-) with about 300 organic molecules is discussed together with the reaction mechanisms. The reactions with phenols, anilines, sulfur compounds (with sulfur atom in lower oxidation state), and molecules with conjugated electron systems are suggested to take place with electron transfer mechanism. The rate constant is high (107–109M-1s-1) when the reduction potential the one-electron oxidized species/molecule couple is well below that of the Cl2•-/2Cl-couple.

Nowadays, increasing extortions regarding environmental problems and energy scarcity have stuck the development and endurance of human society. The issue of inorganic and organic pollutants that exist in water from agricultural, domestic, and industrial activities has directed the development of advanced technologies to address the challenges of water scarcity efficiently. To solve this major issue, various scientists and researchers are looking for novel and effective technologies that can efficiently remove pollutants from wastewater. Nanoscale metal oxide materials have been proposed due to their distinctive size, physical and chemical properties along with promising applications. Cupric Oxide (CuO) is one of the most commonly used benchmark photocatalysts in photodegradation owing to the fact that they are cost-effective, non-toxic, and more efficient in absorption across a significant fraction of solar spectrum. In this review, we have summarized synthetic strategies of CuO fabrication, modification methods with applications for water treatment purposes. Moreover, an elaborative discussion on feasible strategies includes; binary and ternary heterojunction formation, Z-scheme based photocatalytic system, incorporation of rare earth/transition metal ions as dopants, and carbonaceous materials serving as a support system. The mechanistic insight inferring photo-induced charge separation and transfer, the functional reactive radical species involved in a photocatalytic reaction, have been successfully featured and examined. Finally, a conclusive remark regarding current studies and unresolved challenges related to CuO are put forth for future perspectives.

Wastewater contains organic compounds (fatty acids, amino acids, and carbohydrates) that have a significant amount of chemical energy. In this regard, the use of wastewater for recovering energy by some appropriate energy conversion technologies can be considered as an appropriate approach to simultaneously achieve the reduction of environmental contamination and increasing supply of energy. The Photocatalytic Fuel Cell (PFC) can provide a new approach in developing technology for simultaneous organic pollutants removal from wastewaters and power generation, but it also has disadvantages, such as requires higher voltage, more cost and complexity. To present a comprehensive vision of the current state of the art, and progress the treatment efficiency and agitate new studies in these fields, this review discussed the study covering PFC aspects, with a focus on the comparison of pollutant degradation, power generation, different photoanode and photocathode materials as well as the application of the Fenton process in PFCs.

Hierarchical porous poly(L-lactic acid) PLLA@TiO2 fibrous membranes have been successfully fabricated by a facile electrospinning/post-treatment method. The unique blossoming porous structure created by inducing the crystallization of PLLA chains in acetone post-treatment increases the specific surface area and exposes the TiO2 nanoparticles (NPs) on the fiber surface. The porous PLLA@TiO2-0.1 membrane using a PLLA:TiO2 weight ratio of 1:5 achieves the highest photocatalytic efficiency. Methylene blue (MB) is used to observe the removal of contaminants and evidence stable removal kinetics over five cycles under the same conditions. Intriguingly, there is a sine functional relationship between the hydrophobic PLLA@TiO2 membranes measured by the water contact angle (WCA) and the removal kinetic constants k fitted by the experimental data on photocatalytic degradation, which can be used to investigate the mechanism between hydrophobicity and photocatalytic degradation of the membranes. Due to their excellent photocatalytic degradation efficiency, recycling, and stability, porous PLLA@TiO2 fibrous membranes have promising application prospects in photocatalytic water treatment.

Pr-doped CeO2 with different doping levels was prepared from Ce(NO3)3∙6H2O and Pr(NO3)3∙6H2O by solvothermal method without any additional reagents, in which the mixed solution of ethylene glycol and distilled water was employed as a solvent. The influences of Pr-doping on phase composition, crystal structure and morphology were investigated, as well as Pr valence and oxygen vacancy defects. The Pr cations entered into the CeO2 crystal lattice with normal trivalence and formed a Pr-CeO2 solid solution based on the fluorite structure. The larger trivalent Pr was substituted for tetravalent Ce in the CeO2 crystal and compensated by oxygen vacancy defects, which caused the local lattice expansion of the crystal lattice. Moreover, the Pr-doped CeO2 solid solutions exhibited visible color variation from bright cream via brick red to dark brown with the increasing of Pr contents. The degradation of AO7 dye was also investigated using a domestic medical ultraviolet lamp; the removal efficiency of AO7 by 1% and 2% Pr-doped CeO2 approached 100%, much higher than 66.2% for undoped CeO2.

Theoretically, lanthanum can bond with surface oxygens of ZnTiO3 to form La-O-Ti bonds, resulting in the change of both the band structure and the electron state of the surface. To verify this statement, DFT calculations were performed using a model with a dispersed lanthanum atom on the surface (101) of ZnTiO3. The negative heat segmentation values obtained suggest that the incorporation of La on the surface of ZnTiO3 is thermodynamically stable. The bandgap energy value of La/ZnTiO3 (2.92 eV) was lower than that of ZnTiO3 (3.16 eV). TDOS showed that the conduction band (CB) and the valence band (VB) energy levels of La/ZnTiO3 are denser than those of ZnTiO3 due to the participation of hybrid levels composed mainly of O2p and La5d orbitals. From the PDOSs, Bader’s charge analysis, and ELF function, it was established that the La-O bond is polar covalent. MB adsorption on La/ZnTiO3 (−200 kJ/mol) was more favorable than on ZnTiO3 (−85 kJ/mol). From the evidence of this study, it is proposed that the MB molecule first is adsorbed on the surface of La/ZnTiO3, and then the electrons in the VB of La/ZnTiO3 are photoexcited to hybrid levels, and finally, the MB molecule oxidizes into smaller molecules.

Using solar energy to catalyse photo-driven processes to address the energy crisis and environmental pollution plays a role in the path to a sustainable society. Many oxide-based materials, especially perovskite oxides, have been widely investigated as catalysts for photocatalysis in energy and environment because of the low-cost and earth-abundant and good performance. At this stage, there is a need to present a scientific-based evaluation of the technologies developed so far and identify the most sustainable technologies and the existing limitations and opportunities for their commercialisation. This work comprehensively investigated the outcomes using various scientometric indices on perovskite oxide-based photo(electro)catalysts for water splitting, nitrogen fixation, carbon dioxide conversion, organic pollutant degradation, current trends and advances in the field. According to the results achieved, efforts in both energy and environment based on perovskite oxides have been initiated in the 1990s and accelerated since the 2010s. China and the United States were identified as the most contributing countries. Based on the results achieved in this study, the main milestones and current trends in the development of this field have been identified. The aim of this research is to provide useful guidelines for the further investigation of perovskite oxide-based catalysts for photoelectrocatalysis and photocatalysis both in energy and environment on the applications such as water splitting, nitrogen fixation, carbon dioxide conversion, and wastewater treatment.

In this paper, first-principle calculations were performed to investigate the effects of oxygen (O) vacancies (Ovac) on the crystal structure, electronic distribution, adsorption energies of O2 and H2O and the density of states (DOS) of monoclinic bismuth vanadate (m-BiVO4). Ovac were stable when incorporated into m-BiVO4(001) and increased the adsorption energy of O2. Ovac changed the V3d orbitals of m-BiVO4(001) by adding a new band gap level, causing the redundant electrons of V atoms to become carriers and promoting the separation efficiency of electrons and holes. To verify the first-principle calculations, m-BiVO4 with different Ovac levels was prepared via hydrothermal synthesis. X-ray diffraction (XRD) patterns confirmed the existence of the (001) crystal surface of m-BiVO4. In addition, X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) spectroscopy of m-BiVO4 confirmed the presence of Ovac and demonstrated that, as the Ovac level increased, the number of superoxide radicals (O2-·) and hydroxyl radicals (·OH) produced increased. In addition, m-BiVO4 with a higher Ovac level possessed superior photocatalytic properties to and degraded rhodamine B (RhB) dye nearly 2-fold faster than m-BiVO4 with a lower Ovac level. Finally, the removal rate of RhB increased from 23 to 44%. All experimental results were in good agreement with the first-principle calculated results.

In this paper, first-principle calculations were performed to investigate the effects of oxygen (O) vacancies (Ovac) on the crystal structure, electronic distribution, adsorption energies of O2 and H2O and the density of states (DOS) of monoclinic bismuth vanadate (m-BiVO4). Ovac were stable when incorporated into m-BiVO4(001) and increased the adsorption energy of O2. Ovac changed the V3d orbitals of m-BiVO4(001) by adding a new band gap level, causing the redundant electrons of V atoms to become carriers and promoting the separation efficiency of electrons and holes. To verify the first-principle calculations, m-BiVO4 with different Ovac levels was prepared via hydrothermal synthesis. X-ray diffraction (XRD) patterns confirmed the existence of the (001) crystal surface of m-BiVO4. In addition, X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) spectroscopy of m-BiVO4 confirmed the presence of Ovac and demonstrated that, as the Ovac level increased, the number of superoxide radicals (O2-·) and hydroxyl radicals (·OH) produced increased. In addition, m-BiVO4 with a higher Ovac level possessed superior photocatalytic properties to and degraded rhodamine B (RhB) dye nearly 2-fold faster than m-BiVO4 with a lower Ovac level. Finally, the removal rate of RhB increased from 23 to 44%. All experimental results were in good agreement with the first-principle calculated results.

Highlights Current progress in preparations, structures, and physicochemical properties of two-dimensional photo-catalyst materials and environmental remediation.Propose approaches of diverse of two-dimensional photo-catalyst materials-based nanoplatforms, optimization strategies to enhance activity, and their diverse applications.Current challenges and potential advancement of the emerging of two-dimensional photo-catalyst materials., The successful photo-catalyst library gives significant information on feature that affects photo-catalytic performance and proposes new materials. Competency is considerably significant to form multi-functional photo-catalysts with flexible characteristics. Since recently, two-dimensional materials (2DMs) gained much attention from researchers, due to their unique thickness-dependent uses, mainly for photo-catalytic, outstanding chemical and physical properties. Photo-catalytic water splitting and hydrogen (H2) evolution by plentiful compounds as electron (e−) donors is estimated to participate in constructing clean method for solar H2-formation. Heterogeneous photo-catalysis received much research attention caused by their applications to tackle numerous energy and environmental issues. This broad review explains progress regarding 2DMs, significance in structure, and catalytic results. We will discuss in detail current progresses of approaches for adjusting 2DMs-based photo-catalysts to assess their photo-activity including doping, hetero-structure scheme, and functional formation assembly. Suggested plans, e.g., doping and sensitization of semiconducting 2DMs, increasing electrical conductance, improving catalytic active sites, strengthening interface coupling in semiconductors (SCs) 2DMs, forming nano-structures, building multi-junction nano-composites, increasing photo-stability of SCs, and using combined results of adapted approaches, are summed up. Hence, to further improve 2DMs photo-catalyst properties, hetero-structure design-based 2DMs’ photo-catalyst basic mechanism is also reviewed.

Graphical abstract, Highlights • Graphitic carbon nitride (g-C3N4) acts as a promising catalyst for degrading pollutants efficiently. • g-C3N4-based AOPs for treating leachate has been noticed as the high-efficient and feasible approach. • Photocatalytic AOPs can eliminate diverse pollutants and improve the biodegradability of leachate. • The application of g-C3N4 to leachate treatment would be more practical when combined with other emerging AOPs., Landfill leachate poses significant risks to public health via the release of high-toxicity contaminants, including refractory organic compounds, ammonia-nitrogen compounds, and heavy metals. Significant efforts have been made to develop useful methods for leachate disposition and treatment. Advanced oxidation processes (AOPs) are one of the most promising methods, because they can rapidly degrade diverse pollutants and significantly improve the biodegradability of leachate. Graphitic carbon nitride (g-C3N4), a fascinating conjugated polymer, has become a hot topic in AOP research due to its metal-free benefits and high photosensitivity. Thus, combining AOPs with g-C3N4 achieves excellent degradation of refractory pollutants in leachate. Since the composition of leachate is complex in the practical conditions, the information reported by current studies of using g-C3N4 as a remediator is still incomplete and fragmented. Thus, in this review, the recent status of leachate treatment and approaches for its disposal has been summarized and some conclusions have been drawn. In addition, a brief introduction to g-C3N4 and its application in AOPs for leachate treatment have been critically discussed and with its future outlook assessed. Although the development of g-C3N4 in AOPs for leachate treatment is highly efficient and practical, comprehensive study about its application and technology expansion is urgently needed, based on the complex operating conditions. Perspectives on the treatment of leachate using g-C3N4-AOPs are also included. The information and perspectives provided in this review will provide guidance and novel understanding to accelerate the development of g-C3N4-based AOPs for leachate treatment.

A novel graphitic carbon nitride (g-C3N4)–CaTiO3 (CTCN) organic–inorganic heterojunction photocatalyst was synthesized by a facile mixing method, resulting in the deposition of CaTiO3 (CT) nanoflakes onto the surface of g-C3N4 nanosheets. The photocatalytic activity of the as-synthesized heterojunction (along with the controls) was evaluated by studying the degradation of an aqueous solution of rhodamine B (RhB) under UV, visible and natural sunlight irradiation. The CTCN heterojunction with 1:1 ratio of g-C3N4/CT showed the highest photocatalytic activity under sunlight irradiation and was also demonstrated to be effective for the degradation of a colorless, non-photosensitizing pollutant, bisphenol A (BPA). The superior photocatalytic performance of the CTCN heterojunction could be attributed to the appropriate band positions, close interfacial contact between the constituents and extended light absorption (both UV and visible region), all of which greatly facilitate the transfer of photogenerated charges across the heterojunction and inhibit their fast recombination. In addition, the two-dimensional (2D) morphology of g-C3N4nanosheets and CT nanoflakes provides enough reaction sites due to their larger surface area and enhances the overall photocatalytic activity. Furthermore, the active species trapping experiments validate the major role played by superoxide radicals (O2−•) in the degradation of pollutants. Based on scavenger studies and theoretically calculated band positions, a plausible mechanism for the photocatalytic degradation of pollutants has been proposed and discussed.

Fabrication of the heterojunction composites photocatalyst has attained much attention for solar energy conversion due to their high optimization of reduction-oxidation potential as a result of effective separation of photogenerated electrons-holes pairs. In this review, the background of photocatalysis, mechanism of photocatalysis, and the several researches on the heterostructure graphitic carbon nitride (g-C3N4) semiconductor are discussed. The advantages of the heterostructure g-C3N4 over their precursors are also discussed. The conclusion and future perspectives on this emerging research direction are given. This paper gives a useful knowledge on the heterostructure g-C3N4 and their photocatalytic mechanisms and applications. Impact Statements The paper on g-C3N4 Nano-based photocatalysts is expected to enlighten scientists on precise management and evaluating the environment, which may merit prospect research into developing suitable mechanism for energy, wastewater treatment and environmental purification.

The development of microdischarges and the inception dynamics of subsequent microdischarges in an electrode arrangement consisting of a metal pin and a hemispherical dielectric-covered electrode, operated in air with a small toluene admixture, is studied. The discharge is operated with sinusoidal high voltage. A gated ICCD camera and a current probe enable the recording of images and current pulses of the single microdischarges, respectively, while the spatio-temporally resolved development is measured with a multi-dimensional time-correlated single photon counting technique. The overall discharge dynamics changes significantly if a concentration of 35 ppm toluene is added to dry air. A lower high voltage amplitude than in dry air is needed for stable discharge operation. This can be explained by the lower ionization energy of toluene compared to molecular oxygen and nitrogen. The microdischarge development is the same with or without admixture, i.e. a positive (cathode directed) streamer mechanism is observed. Lower mean power is dissipated into the discharge when toluene is admixed. The main effect caused by toluene admixture is the suppression of high-energy microdischarges in case of the cathodic pin half-cycle of the sinusoidal high voltage. The influence on the inception voltage by additional ionization mechanisms and volume memory effects, the consumption of energetic electrons for toluene decomposition reactions, and the modification of the surface by plasma treatment are discussed as possible reasons.

This work reviews an eco-friendly process for producing TiO2 via colloidal aqueous sol–gel synthesis, resulting in crystalline materials without a calcination step. Three types of colloidal aqueous TiO2 are reviewed: the as-synthesized type obtained directly after synthesis, without any specific treatment; the calcined, obtained after a subsequent calcination step; and the hydrothermal, obtained after a specific autoclave treatment. This eco-friendly process is based on the hydrolysis of a Ti precursor in excess of water, followed by the peptization of the precipitated TiO2. Compared to classical TiO2 synthesis, this method results in crystalline TiO2 nanoparticles without any thermal treatment and uses only small amounts of organic chemicals. Depending on the synthesis parameters, the three crystalline phases of TiO2 (anatase, brookite, and rutile) can be obtained. The morphology of the nanoparticles can also be tailored by the synthesis parameters. The most important parameter is the peptizing agent. Indeed, depending on its acidic or basic character and also on its amount, it can modulate the crystallinity and morphology of TiO2. Colloidal aqueous TiO2 photocatalysts are mainly being used in various photocatalytic reactions for organic pollutant degradation. The as-synthesized materials seem to have equivalent photocatalytic efficiency to the photocatalysts post-treated with thermal treatments and the commercial Evonik Aeroxide P25, which is produced by a high-temperature process. Indeed, as-prepared, the TiO2 photocatalysts present a high specific surface area and crystalline phases. Emerging applications are also referenced, such as elaborating catalysts for fuel cells, nanocomposite drug delivery systems, or the inkjet printing of microstructures. Only a few works have explored these new properties, giving a lot of potential avenues for studying this eco-friendly TiO2 synthesis method for innovative implementations.

ZnO is an exciting material for photocatalysis applications due to its high activity, easy accessibility of raw materials, low production costs, and nontoxic. Several ZnO nano and microstructures can be obtained, such as nanoparticles, nanorods, micro flowers, microspheres, among others, depending on the preparation method and conditions. ZnO is a wide bandgap semiconductor presenting massive recombination of the generated charge carriers, limiting its photocatalytic efficiency and stability. It is common to mix it with metal, metal oxide, sulfides, polymers, and nanocarbon-based materials to improve its photocatalytic behavior. Therefore, ZnO–nanocarbon composites formation has been a viable alternative that leads to new, more active, and stable photocatalytic systems. Mainly, graphene is a well-known two-dimensional material, which could be an excellent candidate to hybridize with ZnO due to its excellent physical and chemical properties (e.g., high specific surface area, optical transmittance, and thermal conductivity, among others). This review analyses ZnO–graphene nanocomposites’ recent advances, addressing the synthesis methods and the resulting structural, morphological, optical, and electronic properties. Moreover, we examine the ZnO–graphene composites’ role in the photocatalytic degradation of organic/inorganic pollutants.

Vertical Agx/TiO2 nanorods were successfully grown by a simple oxidation method of a Ti-Ag coating. The samples were grown in the phase of ceramic-like materials, which can be reusable for many cycles for photocatalysis applications. These ceramic-like Agx/TiO2 nanostructures were prepared by the spin-coating of silver nitrate onto Ti sheets. The presence of silver on the surface of the Ti sheet during the oxidation process helped in the growth of one-dimensional nanostructures. The physical properties of the fabricated ceramic-like nanostructures were studied by varying the concentration of silver on the Ti-sheet before the oxidation. One-dimensional nanostructures with an average size varying within the range of 200&ndash, 500 nm were grown. The presence of silver made the nanostructure vertically directed. The nanorods were dense at the low and medium concentrations of 5, 10, and 20 mM of silver in contrary to high silver concentrations, where the nanorods were very sparse at 40 mM. Structural analysis showed the anatase and rutile structure of pure TiO2 with distinguishing diffraction lines A(101) and R(110), however, Agx/TiO2 showed a dominant orientation of A(101), confirming the 1D growth. Raman spectra confirmed the presence of TiO2 via the observation of its corresponding phonon modes. The photocatalysis properties of the fabricated ceramic-like nanostructures were performed on methylene blue (MB) as a known target dye. The low- and medium-silver-concentration samples showed a high photocatalytic activity compared to the pure and high-silver-concentration samples.

The exploration of cost-effective and highly efficient photocatalysts is still a great challenge. In this work, a cost-effective and highly active Bi2WO6/calcined mussel shell (CMS/BWO) composite photocatalyst was prepared by a facile solvothermal route, in which Bi2WO6 nanosheets were tightly, evenly, and vertically grown on waste calcined mussel shells (CMS). Multiple techniques are adopted to characterize the phases, morphology, and chemical properties of the as-fabricated catalysts. In contrast to the stacked Bi2WO6, CMS/BWO has numerous exposed edges and open transfer pathways, which can create more open space and reactive sites for photocatalytic reactions. Such favorable characteristics enable CMS/BWO to efficiently degrade organic pollutants (e.g., rhodamine B (RhB), methylene blue (MB), tetracycline hydrochloride (TC)) under visible light. Moreover, the generation of reactive species during the photocatalytic process is also examined by trapping experiments, disclosing the pivotal role of photo-generated holes (h+) and hydroxyl radicals (&bull, OH) in the photo-degradation of pollutants. Above all, this study not only provides an efficient photocatalyst for environmental remediation, but it also opens up new possibilities for waste mussel shell reutilization.

International audience; A new layered double hydroxide (LDH)-based nanocomposite functionalized with an octahedral molybdenum atom cluster (MC) exhibiting prominent photoactive and oxidation properties was synthesized. Zn[sbnd]Al LDH and Zn[sbnd]Al LDH intercalated dodecyl sulfate compounds (abbreviated as LDH-1 and LDH-2 respectively) were prepared by the co-precipitation method in an aqueous solution. The MCs were simply introduced into the LDH-2 by an anion exchangeable method in dimethylformamide under ambient conditions. The extension of the basal spacing of the LDH-1 from 0.9 nm to about 5 nm by intercalating dodecyl sulfate and Mo6 cluster was confirmed by several complementary technics. The octahedral structure of the Mo6 cluster was retained on the outer surface between big nanosheets (NSs) and inner surface between the single layers that were confirmed by ultraviolet-visible absorption and photoluminescence experiments. The possible chemical bonding between the [Mo6Cli8Cla6-x-y(H2O)ax(OH)ay]x-2 (x = 0, 1 or 2 and y = 0, 1, 2, 3; x + y = 3) clusters and LDH-2 was suggested on the basis of by X-ray photoelectron spectroscopy. The excellent photoactive and oxidation performance of the Mo6 cluster on the methylene blue degradation in an aqueous solution was determined in the dark, under UV light (λ =370 nm) or with the existence of H2O2. The combination of the LDH-2 with a high absorbability and recyclability and the Mo6 cluster will be a promising candidate as a heterogenized homogeneous catalyst for removing organic pollutants. © 2020 Elsevier B.V.

Two-dimensional (2D) transition metal oxide and chalcogenide (TMO&C)-based photocatalysts have recently attracted significant attention for addressing the current worldwide challenges of energy shortage and environmental pollution. The ultrahigh surface area and unconventional physiochemical, electronic and optical properties of 2D TMO&Cs have been demonstrated to facilitate photocatalytic applications. This review provides a concise overview of properties, synthesis methods and applications of 2D TMO&C-based photocatalysts. Particular attention is paid on the emerging strategies to improve the abilities of light harvesting and photoinduced charge separation for enhancing photocatalytic performances, which include elemental doping, surface functionalization as well as heterojunctions with semiconducting and conductive materials. The future opportunities regarding the research pathways of 2D TMO&C-based photocatalysts are also presented.

Single semiconductors such as KTaO3, CdS MoS2 or their precursor solutions were combined to form novel binary and ternary semiconductor nanocomposites by the calcination or by the hydro/solvothermal mixed solutions methods, respectively. The aim of this work was to study the influence of preparation method as well as type and amount of the composite components on the surface properties and photocatalytic activity of the new semiconducting photoactive materials. We presented different binary and ternary combinations of the above semiconductors for phenol and toluene photocatalytic degradation and characterized by X-ray powder diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) specific surface area and porosity. The results showed that loading MoS2 onto CdS as well as loading CdS onto KTaO3 significantly enhanced absorption properties as compared with single semiconductors. The highest photocatalytic activity in phenol degradation reaction under both UV-Vis and visible light irradiation and very good stability in toluene removal was observed for ternary hybrid obtained by calcination of KTaO3, CdS, MoS2 powders at the 10:5:1 molar ratio. Enhanced photoactivity could be related to the two-photon excitation in KTaO3-CdS-MoS2 composite under UV-Vis and/or to additional presence of CdMoO4 working as co-catalyst.

The review explores the feasibility of simultaneous removal of pathogens and chemical pollutants by solar-enhanced advanced oxidation processes (AOPs). The AOPs are based on in-situ generation of reactive oxygen species (ROS), most notably hydroxyl radicals •OH, that are capable of destroying both pollutant molecules and pathogen cells. The review presents evidence of simultaneous removal of pathogens and chemical pollutants by photocatalytic processes, namely TiO2 photocatalysis and photo-Fenton. Complex water matrices with high loads of pathogens and chemical pollutants negatively affect the efficiency of disinfection and pollutant removal. This is due to competition between chemical substances and pathogens for generated ROS. Other possible negative effects include light screening, competitive photon absorption, adsorption on the catalyst surface (thereby inhibiting its photocatalytic activity), etc. Besides, some matrix components may serve as nutrients for pathogens, thus hindering the disinfection process. Each type of water/wastewater would require a tailor-made approach and the variables that were shown to influence the processes—catalyst/oxidant concentrations, incident radiation flux, and pH—need to be adjusted in order to achieve the required degree of pollutant and pathogen removal. Overall, the solar-enhanced AOPs hold promise as an environmentally-friendly way to substitute or supplement conventional water/wastewater treatment, particularly in areas without access to centralized drinking water or sewage/wastewater treatment facilities.

Mixed phase nanocrystalline TiO2 powders (anatase-rutile) (Degussa P25) were prepared by hydrothermal modification. The preparation procedure took place at 200 ° C for 1-10 days in an autoclave system with water as the solvent. Thus, different degrees of modification were achieved. TiO2 water modified nanocrystalline thin films were immobilized on glass substrates by applying a doctor-blade's deposition technique. A variety of spectroscopic [UV-vis reflectance, infra-red (IR), Raman, structural X-ray diffraction (XRD), N-2 absorption (BET)] and microscopic [atomic force microscopy (AFM), scanning electron microscopy (SEM)] techniques were applied to characterize the modified films. A model textile industry pollutant (methyl orange) was used in order to evaluate the photocatalytic efficiency of the modified material. Our results show that the photocatalytic activity of the modified films is improved by a factor of 2 when we extend the hydrothermal treatment up from 1 to about 4 days in the autoclave system. Scratch tests revealed favorable interconnection of the titania nanoparticles as well as significantly higher adhesion to the glass substrate for the modified films, in comparison to the original P25 material. © 2005 Elsevier B.V. All rights reserved. Catalysis Today

Aims: This study was carried out to further characterize fungal species that could degrade 3-chloropropionic acid (3CP)as sole source of carbon and energy. Methodology and Results: Both fungi were able to grow on 3CP after 10 days on solid minimal media. Based on sequencing of its segment of 18S rRNA these isolates were identified as Mucor sp. SP1 and Trichoderma sp. SP2. The isolated strains were not able to grow on media plates containing 10 mM of 2,2-dichloropropionate (2,2DCP) as sole source of carbon. 3CP degradation was observed in liquid minimal medium containing 10 mM 3CP after 18 days culture period. The chloride ion released was detected in both growth medium containing Mucor sp. SP1 and Trichoderma sp. SP2. At least 80% of 10 mM 3CP was utilized in the growth medium. Conclusion, significance and impact of study: Dehalogenase enzyme that can degrade α-chloro-substituted haloalkanoic acids for example 2,2DCP is well studied up to protein crystallization. Very few reports on the degradation of β-chloro-substituted haloalkanoic acids such as 3CP and none from fungi. This study is considered important because it can be compared to that of well-documented α-chloro-substituted haloalkanoic acids degradation. This is the first study to indicate fungal growth on 3CP as sole carbon and energy sources.

A proposal for modelling photo-Fenton reactors for water pollution remediation is presented. Reactor models, based on chemical reaction engineering principles and radiative energy transport fundamentals in homogeneous systems, are derived at both laboratory and solar pilot-plant scales. The proposed methodology is illustrated by presenting an example on the modelling and scaling-up of a solar reactor for degradation of a model pollutant in aqueous solution: the herbicide 2,4-dichlorophenoxyacetic acid. Firstly, a kinetic model derived from a reaction sequence is proposed and its kinetic parameters estimated, using an isothermal, well-stirred tank laboratory photoreactor. Afterwards, the kinetic model is employed to predict the reacting species concentrations during the photo-Fenton degradation in a pilot-plant, nonisothermal solar reactor designed to capture the UV/Visible/IR solar radiation. This approach has proved to be appropriate to simulate the behaviour of the photo-Fenton reactor under different experimental conditions. Fil: Alfano, Orlando Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina Fil: Albizzati, Enrique Donato. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina Fil: Conte, Leandro Oscar. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina

This study presents the performance of GF-mats loaded with TiO2 and Cu under solar/visible light leading to bacterial inactivation and pollutant degradation at both solid-air and solid-liquid interfaces. The GF-mats show effective water disinfection, self-cleaning and degradation of an organic pollutant in solution. Cleaning of the GF-mats was found to be a necessary step before grafting TiO2 and Cu/CuO in amounts of TiO2 (10%-25% by weight) and Cu (0.03%-0.45% by weight) respectively. A GF-mat consisting of 15.4% TiO2 and 0.45% Cu led to bacterial disinfection within similar to 30 min under solar irradiation (290-800 nm light) and within similar to 60 min under visible light irradiation (400-800 nm). The oxidative radicals generated on the TiO2-Cu surface leading to disinfection, self-cleaning and abatement of the pollutant were identified and the diffusion length from the GF-mat was estimated for the most active HO2 center dot radical. The pH/surface potential changes in solution during the degradation of methylene blue (MB), which was taken as a model pollutant, were followed by means of a microelectrode. A GF-mat loaded with TiO2 13.1% and Cu 0.03% by weight led to the degradation of a dilute pollutant solution within similar to 100 min. The pollutant degradation was assessed by high performance liquid chromatography (HPLC) by following the decrease of the intensity of its characteristic absorbance peaks. The TiO2 and Cu eluted from the mat during the degradation of MB were detected by inductively coupled plasma mass-spectrometry (ICP-MS). The surface properties of the mats were investigated by scanning electron microscopy (SEM). Evidence is presented for the redox events on the GF-TiO2-Cu mats during the self-cleaning reactions by XPS. (C) 2017 Elsevier B.V. All rights reserved.

Electrochemically fabricated magnetic mesoporous CoNi@Pt nanorods are excellent nanomotors with controlled magnetic propulsion and excellent catalytic properties. The core–shell structure allows a double functionality: (i) controlled motion of the nanorods by applying rotating magnetic fields at different frequencies and field strengths and (ii) effective catalytic activity of the platinum shell for reactions involving sodium borohydride. The structure and magnetic properties of the CoNi core are not modified by the presence of the Pt shell. Nanorods were propelled via a tumbling-like dynamic by a rotating magnetic field. While in absence of NaBH4, nanorods move at constant speed showing a linear path; in the presence of NaBH4, they showed an intermittent trajectory. These catalytic nanorods can be used as nanocleaners with controlled directionality for pollutants degradation in the presence of borohydride. Their magnetic character allows control of the velocity and the direction throughout the contaminated solution by degrading the different pollutants in their path. The magnetic character of nanorods also allows their easy recycling.

International audience; In this study, the photocatalytic activities were investigated for the treatment of Reactive Green 12 (RG 12) solution under UV and visible irradiation using Cu doped TiO2, and TiO2 impregnated on (1) cellulose and (2) UV-C activated polyester catalysts. The obtained results revealed that TiO2 impregnated on UV-C activated polyester showed promising performances compared to the other synthesized catalysts. Moreover, the dispersion of active sites on UV-C pretreated polyester was optimized and tested for RG 12 removal in the binary mixture, the presence of Direct Red 89 (DR 89) dye had an inhibiting effect on the rate of RG 12 discoloration process because of the competitive effect between dyes molecules toward the available active sites. The role and contribution of reactive oxidizing species (ROS) [rad]OH, O2[rad]− and h+ was also examined with the two catalysts under different light sources; it was found that the superoxide radical anion played the key role in RG 12 photocatalytic degradation for both TiO2 supported catalysts. Nevertheless, the behavior of O2[rad]− radicals was found to be changed from promoting effect to inhibitory effect when changing light from UV to Visible. © 2018 Elsevier B.V.