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The binary heterostructured semiconducting visible light photocatalyst of the iron-doped graphitic carbon nitride/bismuth molybdate (Fe-g-C3N4/Bi2MoO6) composite was prepared by coupling with Fe-doped g-C3N4 and Bi2MoO6 particles. In the present study, a comparison of structural characteristics, optical properties, and photocatalytic degradation efficiency and activity between Fe-doped g-C3N4 particles, Bi2MoO6 particles, and Fe-g-C3N4/Bi2MoO6 composite was investigated. The results of X-ray diffraction (XRD) examination indicate that the hydrothermal Bi2MoO6 particles have a single orthorhombic phase and Fourier transform infrared (FTIR) spectroscopy analysis confirms the formation of Fe-doped g-C3N4. The optical bandgaps of the Fe-doped g-C3N4 and Bi2MoO6 particles are 2.74 and 2.73 eV, respectively, as estimated from the Taut plots obtained from UV-Vis diffuse reflectance spectroscopy (DRS) spectra. This characteristic indicates that the two semiconductor materials are suitable for absorbing visible light. The transmission electron microscopy (TEM) micrograph reveals the formation of the heterojunction Fe-g-C3N4/Bi2MoO6 composite. The results of photocatalytic degradation revealed that the developed Fe-g-C3N4/Bi2MoO6 composite photocatalyst exhibited significantly better photodegradation performance than the other two single semiconductor photocatalysts. This property can be attributed to the heterostructured nanostructure, which could effectively prevent the recombination of photogenerated carriers (electron–hole pairs) and enhance photocatalytic activity. Furthermore, cycling test showed that the Fe-g-C3N4/Bi2MoO6 heterostructured photocatalyst exhibited good reproducibility and stability for organic dye photodegradation. [ABSTRACT FROM AUTHOR]

Although dicofol has been widely banned all over the world as a kind of organochlorine contaminant, it still exists in the environment. This study developed a high-performance liquid chromatography coupled with mass spectrometry (HPLC-MS/MS) detection technique for dicofol, an environmental pollutant, for the first time using in-source fragmentation. The results confirmed that m/z 251 was the only precursor ion of dicofol after in-source fragmentation, and m/z 139 and m/z 111 were reasonable product ions. The main factors triggering the in-source fragmentation were the H+ content and solution conductivity when dicofol entered the mass spectrometer. Density functional theory can be used to analyze and interpret the mechanism of dicofol fragmentation reaction in ESI source. Dicofol reduced the molecular energy from 8.8 ± 0.05 kcal/mol to 1.0 ± 0.05 kcal/mol, indicating that the internal energy release from high to low was the key driving force of in-source fragmentation. A method based on HPLC-MS/MS was developed to analyze dicofol residues in environmental water. The LOQ was 0.1 μg/L, which was better than the previous GC or GC-MS methods. This study not only proposed an HPLC-MS/MS analysis method for dicofol for the first time but also explained the in-source fragmentation mechanism of compounds in ESI source, which has positive significance for the study of compounds with unconventional mass spectrometry behavior in the field of organic pollutant analysis and metabonomics. [ABSTRACT FROM AUTHOR]

Active photocatalysts with an efficiency of 99% were prepared for the degradation of the industrial dye, methylene blue (MB), under visible light irradiation. These photocatalysts comprised Co/Ni-metal–organic frameworks (MOFs), to which bismuth oxyiodide (BiOI) was added as a filler to prepare Co/Ni-MOF@BiOI composites. The composites exhibited remarkable photocatalytic degradation of MB in aqueous solutions. The effects of various parameters, including the pH, reaction time, catalyst dose, and MB concentration, on the photocatalytic activity of the prepared catalysts were also evaluated. We believe that these composites are promising photocatalysts for the removal of MB from aqueous solutions under visible light. [ABSTRACT FROM AUTHOR]

The current work focuses on the photo degradation of organic pollutants, particularly methylene blue (MB) dye, and the production of hydrogen as green energy using a composite of silver phosphate Ag3PO4 (AP) and barium oxide/silver phosphate BaO@Ag3PO4 (APB) as a photocatalyst. This composite was successfully synthesized using a chemical co-precipitation approach. The physicochemical properties of the obtained samples were investigated using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis/DRS), and photoluminescence (PL) spectrophotometry. From XRD, the average crystallite sizes of AP and APB are 39.1 and 46 nm, respectively, with a homogeneous morphology detected by SEM. UV and PL experiments showed that the compound is active under visible light, with an improvement in the lifetimes of the electrons and the holes in the presence of BaO with Ag3PO4. The as-synthesized APB photocatalyst sample showed a remarkably high degradation efficiency of MB (20 ppm, 50 mL) of around 94%, with a hydrogen production yield of around 7538 μmol/(h·g), after 120 min of illumination, which is greater than the degradation efficiency of the AP photocatalyst sample, which was about 88%. The high photodegradation efficiency was attributed to the electronic promotion effect of the BaO particles. The APB composite demonstrated an increased photocatalytic performance in effectively degrading an organic dye (MB) with no secondary pollutants when exposed to visible light irradiation. [ABSTRACT FROM AUTHOR]

The preparation of metal organic frameworks (MOFs) has come to the forefront in recent years because of their outstanding physical and chemical properties. Many MOFs such as Zn, Co, Ni, Fe, and Ag, etc., have been successfully synthesized. In this work, we followed the solvothermal assisted route to synthesize Ag-MOF (abbreviated as AMOF) nanosheets and then applied them as a photocatalyst to remove different organic pollutants, namely methyl orange (MO), crystal violet (CV), and methylene blue (MB). Chemical composition, optical properties, morphology, and microstructural analysis were analyzed using XPS, UV-visible spectrophotometer, FESEM, TEM, and EDS, respectively. The structural properties of AMOF nanosheets were studied by X-ray diffraction (XRD). Nitrogen adsorption and desorption isotherm analysis were utilized to evaluate the specific surface area and pore size of the AMOF nanosheets. Further, AMOF nanosheets showed notable photocatalytic performance for various dye pollutants degradation. The results confirmed 74.5, 85.5, and 90.7% of MO, CV, and MB dye pollutants removal after 120 min of irradiation with the rate constants (k) of 0.0123, 0.0153, and 0.0158 min−1, respectively. The effect of superoxide radicals (O2−) and photogenerated holes (h+) on the organic dye pollutants removal was investigated using radical scavenger trapping studies. Moreover, the stability study also confirmed the recyclability of the photocatalyst. Therefore, the findings of this research present a realizable method to grow AMOF photocatalyst for successful degradation of various dye pollutants. [ABSTRACT FROM AUTHOR]

Biochars are considered as promising materials in energy storage and environmental remediation because of their unique physicochemical properties and low cost. However, the fabrication of multifunctional biochar materials with a well-developed hierarchical porous structure as well as self-doped functionalities via a facile strategy remains a challenge. Herein, we demonstrate a heteroatom-doped porous biochar, prepared by a hydrothermal pretreatment followed by a molten salt activation route. With the creation of a high specific surface area (1501.9 m2/g), a hierarchical porous structure, and the incorporation of oxygen-/nitrogen-functional groups, the as-prepared biochar (BC-24) exhibits great potential for supercapacitor application and organic pollutant elimination. The assembled biochar electrode delivers a specific capacitance of 378 F/g at 0.2 A/g with a good rate capability of 198 F/g at 10 A/g, and excellent cycling stability with 94.5% capacitance retention after 10,000 recycles. Moreover, BC-24 also exhibits superior catalytic activity for phenol degradation through peroxydisulfate (PDS) activation. The phenol (0.2 mM) can be effectively absorbed and then completely degraded within only 25 min over a wide pH range with low catalyst and PDS dosages. More importantly, TOC analysis indicates 81.7% of the phenol is mineralized within 60 min, confirming the effectiveness of the BC-24/PDS system. Quenching experiments and EPR measurements reveal that SO4·− and ·OH as well as 1O2 are involved in the phenol degradation, while the non-radical pathway plays the dominant role. This study provides valuable insights into the preparation of cost-effective carbon materials for supercapacitor application and organic contaminant remediation. [ABSTRACT FROM AUTHOR]

Environmental biotechnologies are a popular choice for using efficient, low-cost, low-waste, and environmentally friendly methods to clean up and restore polluted sites. In these technologies, plants (terrestrial and aquatic) and their associated micro-organisms are used to eliminate pollutants that threaten the health of humans and animals. They have emerged as alternative methods to conventional techniques that have become increasingly aggressive to the environment. Currently, all actors of the environment, whether governors, industrialists, or citizen associations are more interested in the application and development of these technologies. The present overview provides available information about recent developments in phytoremediation processes using specifically aquatic plants. The main goal is to highlight the key role of this technology in combating the drastic organic and inorganic pollution that threatens our planet daily. Furthermore, this study presents the valorization of aquatic plant after phytoremediation process in energy. In particular, this article tries to identify gaps that are necessary to propose future developments and prospects that could guarantee sustainable development aspired by all generations. [ABSTRACT FROM AUTHOR]

Peroxidase-like nanozymes are nanoscale materials that can closely mimic the activity of natural peroxidase for a range of oxidation reactions. Surface coating with polymer nanogels has been considered to prevent the aggregation of nanozymes. For a long time, the understanding of polymer coating has been largely limited to its stabilization effect on the nanozyme in aqueous media, while little is known about how polymer coating plays a role in interaction with substrates and primary oxidants to dictate the catalytic process. This work reported a facile sequential modification of Fe3O4 nanoparticles to polyacrylamide coated nanozymes, and as low as 112 mg/L samples with only 5 mg/L Fe3O4 could nearly quantitatively (99%) remove a library of organic dyes with either H2O2 or Na2S2O8 as primary oxidants. The catalytic results and molecular simulation provide both experimental and computational evidence that the hydrogen bonding interaction between the reactant and nanozymes is key for the high local concentration hence catalytic efficiency. We envision that this work, for the first time, provides some insights into the role of polymer coating in enhancing the catalytic activity of nanozyme apart from the well-known water dispersity effect. [ABSTRACT FROM AUTHOR]

Semiconductor photocatalysis is considered to be a promising technique to completely eliminate the organic pollutants in wastewater. Recently, S-scheme heterojunction photocatalysts have received much attention due to their high solar efficiency, superior transfer efficiency of charge carriers, and strong redox ability. Herein, we fabricated an S-scheme heterostructure BiOCl/MoSe2 by loading MoSe2 nanosheets on the surface of BiOCl microcrystals, using a solvothermal method. The microstructures, light absorption, and photoelectrochemical performances of the samples were characterized by the means of SEM, TEM, XRD, transient photocurrents, electrochemical impedance, and photoluminescence (PL) spectra. The photocatalytic activities of BiOCl, MoSe2, and the BiOCl/MoSe2 samples with different MoSe2 contents were evaluated by the degradation of methyl orange (MO) and antibiotic sulfadiazine (SD) under simulated sunlight irradiation. It was found that BiOCl/MoSe2 displayed an evidently enhanced photocatalytic activity compared to single BiOCl and MoSe2, and 30 wt.% was an optimal loading amount for obtaining the highest photocatalytic activity. On the basis of radical trapping experiments and energy level analyses, it was deduced that BiOCl/MoSe2 follows an S-scheme charge transfer pathway and •O2−, •OH, and h+ all take part in the degradation of organic pollutants. [ABSTRACT FROM AUTHOR]

In this study, we report the synthesis of a 3-dimensional (3D) hierarchical Bi3O4Cl/Bi5O7I (BOC/BOI) heterostructure for the photocatalytic degradation of Rhodamine-B (RhB) dye and colorless Bisphenol-A (BPA) pollutant under visible light. The heterostructure was prepared using in situ solvothermal and calcination methods. BOC/BOI exhibits a 3D hierarchical structure constructed with thin nano-platelets. The photocatalytic performance of the BOC/BOI photocatalyst demonstrated that the degradation efficiencies of RhB and BPA were 97% and 92% after light illumination within 90 and 30 min, respectively. In comparison, bare BOC and BOI efficiencies were only 20% and 10% for RhB dye, respectively, and 2.3% and 37% for BPA aqueous pollutants, respectively. Moreover, radical trapping measurements indicated that •O2− and •OH radicals played prominent roles in RhB and BPA degradation into mineralization. Analysis of band structures and photochemical redox reactions of BOC/BOI revealed a Z-scheme charge transfer between BOC and BOI by an internal electric field formed at the interface. Therefore, the highly improved photocatalytic performance of the BOC/BOI heterostructure is attributed to the synergetic effects of large surface area, high visible-light absorption, and the enhanced separation and transport of photo-excited electron–hole pairs induced by the hierarchical and Z-scheme heterojunction of the BOC/BOI. [ABSTRACT FROM AUTHOR]

Advanced oxidation processes (AOPs) have become a favored approach in wastewater treatment due to the high efficiency and diverse catalyzed ways. Iron-based materials were the commonly used catalyst due to their environmental friendliness and sustainability in the environment. We collected the published papers relative to the application of the modified iron-based materials in AOPs between 1999 and 2020 to comprehensively understand the related mechanism of modified materials to improve the catalytic performance of iron-based materials in AOPs. Related data of iron-based materials, modification types, target pollutants, final removal efficiencies, and rate constants were extracted to reveal the critical process of improving the catalytic efficiency of iron-based materials in AOPs. Our results indicated that the modified materials through various mechanisms to enhance the catalytic performance of iron-based materials. The principal aim of iron-based materials modification in AOPs is to increase the content of available Fe2+ and enhance the stability of Fe2+ in the system. The available Fe2+ is elevated by the following mechanisms: (1) modified materials accelerate the electron transfer to promote the Fe3+/Fe2+ reaction cycle in the system; (2) modified materials form chelates with iron ions and bond with iron ions to avoid Fe3+ precipitation. We further analyzed the effect of different modifying materials in improving these two mechanisms. Combining the advantages of different modified materials to develop iron-based materials with composite modification methods can enhance the catalytic performance of iron-based materials in AOPs for further application in wastewater treatment. [ABSTRACT FROM AUTHOR]

In this study, TiO2 nanotubes (TNTs) were fabricated on a Ti sheet following the anodic oxidation method and were decorated with reduced graphene oxide (RGO), graphene oxide (GO), and bismuth (Bi) via electrodeposition. The surface morphologies, crystal structures, and compositions of the catalyst were characterized by field emission scanning electron microscopy, Auger electron spectroscopy, X-ray diffraction, photoluminance spectra, X-ray photoelectron spectroscopy, and energy dispersive X-ray spectroscopy. The TNTs loaded with RGO, GO, and Bi were used in a continuous-flow system as photocatalysts for the degradation of methylene blue (MB) dye. It was found that the TNTs are efficient photocatalysts for the removal of color from water; upon UV irradiation on TNTs, the MB removal ratio was ~89%. Moreover, the photocatalytic activities of the decorated TNTs were higher than that of pristine TNTs in visible light. In comparison with TNTs, the rate of MB removal in visible light was increased by a factor of 3.4, 3.2, and 2.9 using RGO-TNTs, Bi-TNTs, and GO-TNTs, respectively. The reusability of the catalysts were investigated, and their quantum efficiencies were also calculated. The cylindrical anodized TNTs were excellent photocatalysts for the degradation of organic pollutants. Thus, it was concluded that the continuous-flow photocatalytic reactor comprising TNTs and modified TNTs is suitable for treating wastewater in textile industries. [ABSTRACT FROM AUTHOR]

This paper proposes an optical method which allows determination of the organic compound concentration in water by measurement of the UV (ultraviolet) absorption at a wavelength of 250 nm~300 nm. The UV absorbance was analyzed by means of a multiple linear regression model for estimation of the total organic carbon contents in water, which showed a close correlation with the UV absorbance, demonstrating a high adjusted coefficient of determination, 0.997. The comparison of the TOC (total organic carbon) concentrations for real samples (tab water, sea, and river) calculated from the UV absorbance spectra, and those measured by a conventional TOC analyzer indicates that the higher the TOC value the better the agreement. This UV absorbance method can be easily configured for real-time monitoring water pollution, and built into a compact system applicable to industry areas. [ABSTRACT FROM AUTHOR]

The present work is considered to investigate the sources, concentration, and composition of polycyclic aromatic hydrocarbons (PAHs) and associated health risk assessment of road dust in Riyadh City, Saudi Arabia. The study region included an urban area, strongly affected by traffic, a bare and an industrial area. A total of 50 locations were selected for sampling and 16 different PAHs were determined. The concentration of PAHs in road dust and their estimated lifetime average daily dose (LADD) for adults (human) ranged from 0.01 to 126 ng g−1 and 1950 to 16,010 mg kg−1 day−1, respectively. The ADDing was calculated separately for children (>6), teenagers (6−12), and adults (>12) for all PAHs with each collected sample. Moreover, the average daily exposure dose by ingestion (ADDing) and average daily exposure dose by dermal absorption (ADDder) were more in children (<6 years) as compared to teenagers (6−12 years) and adults (>12 years). Likewise, total equivalency factor based on BaP (TEQBaP) calculations pointed out that PAHs having more benzene rings or having high molecular weight showed high TEQBaP as compared to low molecular weight PAHs. The data revealed that the children population is at high risk for asthma, respiratory and cardiovascular diseases, and immunity suppression as compared to adults in the particular area of investigated region. These outcomes of this study can be used to deliver significant policy guidelines concerning habitants of the area for possible measures for controlling PAHs contamination in Riyadh City to protect human health and to ensure environmental sustainability.

Increasing trends of environmental pollution and emerging contaminants from anthropogenic activities have urged researchers to develop innovative strategies in wastewater management, including those using the biocatalyst laccase (EC 1.10.3.2). Laccase works effectively against a variety of substrates ranging from phenolic to non-phenolic compounds which only require molecular oxygen to be later reduced to H 2 O as the final product. In this study, we performed a bibliometric analysis on the metadata of literature acquired through the Scopus database (24 October 2022) with keyword combination "Laccase" AND "Pollutant" OR "Wastewater". The included publications were filtered based on year of publication (1978-2022), types of articles (original research articles and review articles) and language (English). The metadata was then exported in a CSV (.csv) file and visualized on VosViewer software. A total of 1865 publications were identified, 90.9% of which were original research articles and the remaining 9.1% were review articles. Most of the authors were from China ( n = 416; 22.3%) and India ( n = 276; 14.79%). In the case of subject area, 'Environmental Science' emerged with the highest published documents ( n = 1053; 56.46%). The identified papers mostly cover laccase activity in degrading pollutants, and chitosan, which can be exploited for the immobilization. We encourage more research on laccase-assisted wastewater treatment, especially in terms of collaborations among organizations.

Peroxydisulfate (PDS) can be activated by electrochemistry, for which using atom H* as an activator is feasibly favorable in theoretical and experimental applications. Studies have shown that atomic H* can cleave the peroxide bond as a single-electron reducing agent in Na 2 S 2 O 8 to generate SO 4 •- , thus achieving the degradation of pollutants. Herein, Pd nanoparticles synthesized by in an in situ solution were dispersed in carbon black and then loaded on carbon felt, called Pd/C@CF, as the cathode for peroxydisulfate activation. This showed an ideal degradation effect on a small electrode (10 mm × 10 mm). Cyclic voltammetry (CV) and linear sweep voltammetry (LSV) tests were taken to verify the significant increase in the yield of the reduction of Na 2 S 2 O 8 by H*. The degradation experiments and free-radical scavenging experiment confirmed that the atomic H* was the dominant component triggering the activation of PDS to generate SO 4 •- . A Pd/C@CF composite electrodes have low pH dependence, high stability and recyclability, etc., which has many potential practical applications in wastewater treatment. In addition, H* can also reduce H 2 O 2 to •OH by breaking the peroxide bond, so the removal of pollutants by the same amount of H 2 O 2 and Na 2 S 2 O 8 under the same conditions is compared, and their application prospects are analyzed and compared.

Dye-containing pollutants are currently a threat to the environment, and it is highly challenging to eliminate these dyes photocatalytically under visible light. Herein, we designed and prepared a ZnO/CuO/g-C3N4 (ZCG) heterostructure nanocomposite by a co-crystallization procedure and applied it to eliminate pollutants from wastewater via a photocatalytic scheme. The structural and morphological features of the composite confirmed the formation of a ZCG nanocomposite. The photocatalytic capability of the ZCG photocatalyst was investigated via the decomposition of methylene blue dye. The outstanding activity level of 97.46% was reached within 50 min. In addition, the proficiency of the ZCG composite was 753%, 392%, 156%, and 130% higher than photolysis, g-C3N4, CuO, and ZnO, respectively. Furthermore, the photodeterioration activity on Congo red was also evaluated and found to be excellent. The enhanced catalytic achievement is attributed to the construction of heterojunctions among the constituent compounds. These properties boost the charge transfer and decrease the recombination rate. Moreover, the reusability of the ZCG product was explored and a negligible photoactivity decline was detected after six successful runs. The outcomes suggest the as-prepared nanocomposite can be applied to remove pollutants, which opens a new door to practical implementation. [ABSTRACT FROM AUTHOR]

Biochar nanoparticles (BC NPs), produced by low temperature pyrolysis (350 °C) of microalgae (Nannochloropsis sp.) and nutshells, are proposed as low-cost and sustainable co-catalysts to promote the photocatalytic activity of TiO2 nanotube (NT) arrays towards the degradation of methylene blue (MB) used as an organic pollutant model molecule. BC NPs (size < 25 nm) were obtained by treating bulk BC (i.e., biomass after pyrolysis) by sonication–centrifugation cycles in a water solution. The filtered BC NPs dispersion was deposited by simple drop-casting on the TiO2 NT support. The BC loading was varied by performing multiple depositions. Photocatalytic experiments under UV light (365 nm) revealed that the decoration with BC NPs significantly improves the TiO2 photoactivity. Such enhancement is mainly influenced by the amount of BC deposited; upon optimizing the BC deposition conditions, the rate of photocatalytic degradation of MB increases approximately three times with respect to bare TiO2, almost irrespective of the nature of the raw material. The greater photocatalytic activity of BC-TiO2 can be attributed to the synergistic combination of reactant/product adsorption and catalytic degradation of the adsorbed organic pollutant, as well as an improved charge carrier separation and electron transfer. [ABSTRACT FROM AUTHOR]

Finding new technologies and materials that provide real alternatives to the environmental and energy-related issues represents a key point on the future sustainability of the industrial activities and society development. The water contamination represents an important problem considering that the quantity and complexity of organic pollutant (such as dyes, pesticides, pharmaceutical active compounds, etc.) molecules can not be efficiently addressed by the traditional wastewater treatments. The use of fossil fuels presents two major disadvantages: (1) environmental pollution and (2) limited stock, which inevitably causes the energy shortage in various countries. A possible answer to the above issues is represented by the photocatalytic technology based on S-scheme heterostructures characterized by the use of light energy in order to degrade organic pollutants or to split the water molecule into its components. The present mini-review aims to outline the most recent achievements in the production and optimization of S-scheme heterostructures for photocatalytic applications. The paper focuses on the influence of heterostructure components and photocatalytic parameters (photocatalyst dosage, light spectra and intensity, irradiation time) on the pollutant removal efficiency and hydrogen evolution rate. Additionally, based on the systematic evaluation of the reported results, several perspectives regarding the future of S-scheme heterostructures were included. [ABSTRACT FROM AUTHOR]

The treatment of organic dye contaminants in wastewaters has now becoming more imperative. Fenton-like degradation of methylene blue (MB) and methyl orange (MO) in aqueous solution was investigated by using a nanostructure that a layer of CuCl2 nanoflake film grown on the top surface of nanoporus anodic alumina substrate (nano-PAA-CuCl2) as catalyst. The new nano-PAA-CuCl2 composite was fabricated with self-assembly approach, that is, a network porous structure film composed of CuCl2 nanoflake grown on the upper surface of nanoporous anodic alumina substrate, and the physical and chemical properties are characterized systematically with the X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and high-resolution transmission electron microscopy (HRTEM), Energy Dispersive Spectrometer (EDS), X-ray photoelectron spectroscopy (XPS). The experimental results showed that the nano-PAA-CuCl2 catalyst presented excellent properties for the degradation of two typical organic pollutants such as MB and MO, which were almost completely degraded with 8 × 10−4mol/L nano-PAA-CuCl2 catalyst after 46 min and 60 min at reaction conditions of H2O2 18 mM and 23 mM, respectively. The effects of different reaction parameters such as initial pH, H2O2 concentration, catalyst morphology and temperature were attentively studied. And more, the stability and reusability of nano-PAA-CuCl2 were examined. Finally, the mechanism of MB and MO degradation by the nano-PAA-CuCl2/H2O2 system was proposed, based on the experimental data of the BCA and the temperature-programmed reduction (H2-TPR) and theoretical analysis, the reaction kinetics belonged to the pseudo-first-order equation. This new nanoporous composite material and preparation technology, as well as its application in Fenton-like reaction, provide an effective alternative method with practical application significance for wastewater treatment. [ABSTRACT FROM AUTHOR]

Along with industrialization and rapid urbanization, environmental remediation is globally a perpetual concept to deliver a sustainable environment. Various organic and inorganic wastes from industries and domestic homes are released into water systems. These wastes carry contaminants with detrimental effects on the environment. Consequently, there is an urgent need for an appropriate wastewater treatment technology for the effective decontamination of our water systems. One promising approach is employing nanoparticles of metal oxides as photocatalysts for the degradation of these water pollutants. Transition metal oxides and their composites exhibit excellent photocatalytic activities and along show favorable characteristics like non-toxicity and stability that also make them useful in a wide range of applications. This study discusses some characteristics of metal oxides and briefly outlined their various applications. It focuses on the metal oxides TiO2, ZnO, WO3, CuO, and Cu2O, which are the most common and recognized to be cost-effective, stable, efficient, and most of all, environmentally friendly for a sustainable approach for environmental remediation. Meanwhile, this study highlights the photocatalytic activities of these metal oxides, recent developments, challenges, and modifications made on these metal oxides to overcome their limitations and maximize their performance in the photodegradation of pollutants. [ABSTRACT FROM AUTHOR]

In this work, artificial oxygenation treatment (pure oxygen aeration or oxygen enriched water injection) combined with the introduction of exogenous microorganisms was employed to purify urban river sediment for the first time. Results showed that the developed in situ remediation strategy could increase the dissolved oxygen (DO) concentration and oxidation-reduction potential (ORP) value of the sediments. Benefiting from the increase of DO concentration, the bacterial diversity was enhanced. The highest removal efficiencies of organic matter were 18.4% and 22.3% through pure oxygen aeration and oxygen enriched water injection, respectively. More importantly, overlying water quality was not affected. By comparison, oxygen enriched water injection treatment could achieve better performance on sediment purification. Introducing exogenous microorganisms further reduced the organic matter content of the sediment. In short, the current work not only proposed a promising strategy for controlling urban river sediment pollution, but also provided novel insight for the understanding of river sediment containing highly concentrated organic matter. [ABSTRACT FROM AUTHOR]

Composite nanomaterials having Ag nanoparticles (NPs) that decorate nanostructured AgCl (Ag/AgCl) are promising as plasmonic photocatalysts because of the visible-light absorption of Ag NPs. However, the narrow absorption bands of Ag NPs near 400 nm cause inefficient absorption in the visible range and, consequently, unsatisfactory photocatalytic activity of Ag/AgCl nanomaterials. In this study, we introduce a new class of AgCl-based photocatalysts that are decorated with bimetallic Ag and Au NPs (AgCl@AgAu NPs) for visible-light-driven photocatalytic degradation of organic pollutants. Polyvinylpyrrolidone induces selective reduction of noble metal precursors on AgCl while leaving AgCl intact. The extended composition of the decorating NPs red-shifts the absorption band to 550–650 nm, which allows the catalysts to take advantage of more energy in the visible range for improved efficiency. Furthermore, we control the structures of the AgCl@AgAu NPs, and investigate their correlation with photocatalytic properties. The versatility, chemical stability, and practical application of the AgCl@AgAu NPs are demonstrated using various organic pollutants, recycling experiments, and natural aqueous media, respectively. Our fundamental investigation on the synthesis and applications of AgCl-based nano-photocatalysts is highly valuable for designing plasmonic photocatalysts and expanding their utilization. [ABSTRACT FROM AUTHOR]

Titanium dioxide (TiO2) and TiO2/copper (denoted as TC) composite were prepared via hydrothermal process. In the meantime, divinylbenzene (DVB) and bismaleimide (BMI) monomers were allowed to participate in in-situ radical polymerization in the presence of azobisisobutyronitrile (AIBN) initiator to afford porous polymers (abridged as PP). The as-obtained PP were mixed together with tetrabutyl titanate (TBT) and CuSO4·5H2O in vacuum to obtain PP/TC composite (denoted as PPTC) containing incorporated TC composite in the pores of PP. The as-prepared TiO2, TC, and PPTC were characterized by transmission electron microscopy, scanning electron microscopy, X-ray diffraction, fluorescence spectrometry, and electron spin resonance spectrometry, and so on. Furthermore, their photocatalytic activity for the degradation of N,N-dimethylformamide, methyl orange, phenol, and methylene blue under the irradiation of simulated sunlight (Xe lamp light) and natural sunlight were investigated. Findings indicated that, whether under simulated sunlight or nature sunlight irradiation, PPTC exhibited much better photocatalytic performance than TiO2 and TC for the degradation of the tested organic pollutants. Particularly, it allowed N,N-dimethylformamide (DMF) to be degraded by a rate of 73.7% under simulated sunlight irradiation and it retained photocatalytic activity even after six cycles of reuse, exhibiting promising potential for the removal of organic pollutants in wastewater (including industrial water, aquaculture wastewater, and domestic sewage). The desired photocatalytic performance of the as-prepared PPTC is attributed to two aspects. Namely, the incorporation of Cu2+ into the fine structure of TiO2 contributes to increasing photocatalyst activity and producing more free radical while the embedding of TC composite into the PP pores improves to the contact area between the photocatalyst and organic pollutants, and both are beneficial for improving the adsorption capacity and activity of the photocatalyst, thereby enhancing the degradation of the organic pollutants. [ABSTRACT FROM AUTHOR]

Screen-printed platforms integrated with molecularly imprinted polymers (MIP) were fabricated and characterized as potentiometric sensors for diquat (DQ). The synthesized MIP beads were studied as sensory carriers in plasticized poly(vinyl chloride) membranes. The sensors were constructed by using poly(3,4-ethylenedioxythiophene) (PEDOT) as solid-contact material to diminish charge-transfer resistance and water layer potential. Conventional ion-selective electrodes (ISEs) with internal filling solution were used for comparison. The designed electrodes showed near Nernstian slopes of 28.2 ± 0.7 (r² = 0.999) over the concentration range of 1.0 × 10 -6 -1.0 × 10 -2 M with the limit of detection 0.026 µg/mL over the pH range 4.2-9.0. The electrode exhibited good selectivity for diquat cations over a large number of organic and inorganic cations. The sensor was successfully introduced for direct measurement of diquat content in commercial pesticide preparations and different spiked potato samples. The results showed that the proposed electrode has a fast and stable response, good reproducibility, and applicability for direct assessment of diquat content. The proposed potentiometric method is simple and accurate in comparison with the reported HPLC methods. Besides, it is applicable to turbid and colored sample solutions., Competing Interests: The authors declare no conflict of interest.

Photocatalysis has recently emerged as an advanced, green, and eco-friendly process for the treatment of wastewater and air, and antimicrobial disinfection applications. In this context, TiO2 nanostructures have been shown to be the prominent photocatalyst candidates due to their low cost, non-toxicity, and ease of fabrication. This review highlights the investigation and development of TiO2 photocatalyst film by sol-gel method with special emphasis on the photodecolorization of synthetic dyes and antibacterial activities. Furthermore, various synthesis methods for the preparation of TiO2 films and their advantages, as well as limitations, are summarized. Finally, recent advances in TiO2 films by sol-gel method for dye degradation and antibacterial activities, challenges, and future perspective are discussed. [ABSTRACT FROM AUTHOR]

The present study investigated the kinetics and formation of hydroxylated and chlorinated intermediates during electrochemical oxidation of salicylic acid (SA). A chloride (NaCl) and sulfate (Na2SO4) electrolyte were used, along with two different anode materials, boron doped diamond (BDD) and platinum (Pt). Bulk electrolysis of SA confirmed the formation of both hydroxylated and chlorinated intermediates. In line with the density functional theory (DFT) calculations performed in this study, 2,5- and 2,3-dihydroxybenzoic acid, 3- and 5- chlorosalicylic acid and 3,5-dichlorosalicylic acid were the dominating products. In the presence of a chloride electrolyte, the formation of chlorinated intermediates was the predominant oxidation mechanism on both BDD and Pt anodes. In the absence of a chloride electrolyte, hydroxylated intermediates prevailed on the Pt anode and suggested the formation of sulfonated SA intermediates on the BDD anode. Furthermore, direct oxidation at the anode surface only played a subordinate role. First order kinetic models successfully described the degradation of SA and the formation of the observed intermediates. Rate constants provided by the model showed that chlorination of SA can take place at up to more than 60 times faster rates than hydroxylation. In conclusion, the formation of chlorinated intermediates during electrochemical oxidation of the organic model pollutant SA is confirmed and found to be dominant in chloride containing waters. [ABSTRACT FROM AUTHOR]

All-solid-state potentiometric sensors were prepared by using polyaniline (PANI) as the solid contact material. A film of PANI (thickness approximately being 0.25 µm) was deposited on a solid substrate (carbon screen printed platform). The PANI layer was subsequently coated with an ion-selective membrane (ISM) containing uniform-sized molecularly imprinted nanoparticles to produce a solid-contact ion-selective electrode (SC/ISE) for bispyribac herbicide (sensor I). In addition, aliquat 336 was also used as an ion exchanger in plasticized PVC membrane (sensor II). The proposed sensors revealed a remarkably improved sensitivity towards bispyribac ions with anionic slopes of −47.8 ± 1.1 (r2 = 0.9995) and −44.4 ± 1.4 (r2 = 0.9997) mV/decade over a linear range 1.0 × 10−2–8.6 × 10−6 M, 1.0 × 10−2–9.0 × 10−6 M and detection limits of 1.33 and 1.81 µg/mL for sensors I and II, respectively.Selectivity of both sensors is significantly high for different common pesticides and inorganic anions. The potential stability of the SC/ISEs was studied using chronopotentiometry. Electrochemical impedance spectrometry was used to understand the charge-transfer mechanisms of the different types of ion-selective electrodes studied. The impedance response of the electrodes was modelled by using equivalent electrical circuits. The sensors were used for a direct measurement of the bispyribac content in commercial herbicide formulations and soil samples collected from agricultural lands planted with rice and sprayed with bispyribac herbicide. The results agree fairly well with data obtained using HPLC method. [ABSTRACT FROM AUTHOR]

A series of composites consisting of g-C3N4 sheet and mesoporous Nb2O5 (mNb2O5) microsphere were fabricated by in situ hydrolysis deposition of NbCl5 onto g-C3N4 sheet followed by solvothermal treatment. The samples were characterized using powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), N2 adsorption-desorption, X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS) and photoluminescence spectroscopy (PL). The photocatalytic activity of the composites was studied by degradation of rhodamine B (RhB) and tetracycline hydrochloride (TC-HCl) in aqueous solution under visible light irradiation (λ > 420 nm). Compared with g-C3N4 and mNb2O5, g-C3N4-mNb2O5 composites have higher photocatalytic activity due to synergistic effect between g-C3N4 and mNb2O5. Among these composites, 4% g-C3N4-mNb2O5 has the highest efficiency and good recyclability for degradation of both RhB and TC-HCl. [ABSTRACT FROM AUTHOR]

This paper proposes an optical method which allows determination of the organic compound concentration in water by measurement of the UV (ultraviolet) absorption at a wavelength of 250 nm~300 nm. The UV absorbance was analyzed by means of a multiple linear regression model for estimation of the total organic carbon contents in water, which showed a close correlation with the UV absorbance, demonstrating a high adjusted coefficient of determination, 0.997. The comparison of the TOC (total organic carbon) concentrations for real samples (tab water, sea, and river) calculated from the UV absorbance spectra, and those measured by a conventional TOC analyzer indicates that the higher the TOC value the better the agreement. This UV absorbance method can be easily configured for real-time monitoring water pollution, and built into a compact system applicable to industry areas.