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Due to the unique properties of heterojunction interfaces, heterojunction materials have broad application prospects in gas sensors. In this work, a facile and economical two-step synthesis method was employed to fabricate h-BN/WO 3 heterojunctions, exhibiting excellent performance in triethylamine (TEA) detection. The results indicate that compared to pure WO 3 sensors, h-BN/WO 3 sensors exhibit superior TEA sensing capabilities, with an excellent response of 281.45 to 20 ppm TEA at 100 °C, which is 3.4 times higher. Moreover, h-BN/WO 3 sensors demonstrate favorable response times, low detection limits, and good stability. These significant enhancements are attributed to the increase in oxygen vacancies and the establishment of heterojunctions between h-BN and WO 3 . Heterojunctions can regulate the concentration and transport rate of charge carriers, as well as the interface potential barrier, thereby affecting the gas sensing processes. This work may promote the further development of sensing materials and the practical application of WO 3 sensors in TEA detection., 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 © 2024 Elsevier Ltd. All rights reserved.)

Herein, coupling of noble metal-free plasmonic copper nanoparticles with tungsten suboxide and supporting on zeolite nanoclay (Cu/WO 3-x @ZNC) composite will be introduced for bi-functional photocatalytic ciprofloxacin (CIP) degradation and water photothermal evaporation under visible/infrared (Vis/IR) exposure. Reduced band-gap of WO 3-x via oxygen vacancies creation and localized surface plasmon resonance (LSPR) formation by Cu nanoparticles contributed significantly the extension and intensification of composite's photo-absorption range. Furthermore, small mesoporous structure of ZNC enhanced CIP adsorption and charge carriers separation where the reported photocatalytic efficiencies were 88.3 and 81.7% upon IR and Vis light exposure respectively. It was evidenced that plasmonic hot electrons (e - .s) and hydroxyl radicals (OH •- ) performed the basic functions of the photocatalytic process. At the other side, oxygen vacancies existence, plasmonic effect, and confining thermal characteristics of WO 3-x , Cu, and ZNC correspondingly induced water photothermal evaporation with efficiencies up to 97.5 and 72.8% under IR and Vis illumination respectively. This work introduces synthesis of a novel bi-functional photocatalytic-photothermal composite by metal sub-oxide and non-noble metal plasmonic coupling and supporting on naturally-derived carrier for water restoration under broad spectral exposure., Competing Interests: Declaration of competing interest No competing financial interests or personal relationships could influence this paper work to be declared., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Water pollution has been made worse by the widespread use of organic dyes and their discharge, which has coincided with the industry's rapid development. Piezoelectric catalysis, as an effective wastewater purification method with promising applications, can enhance the catalyst activity by collecting tiny vibrations in nature and is not limited by sunlight. In this work, we designed and synthesized intriguing WS 2 /Bi 2 WO 6 heterojunction nanocomposites, investigated their shape, structure, and piezoelectric characteristics using a range of characterization techniques, and used ultrasound to accelerate the organic dye Rhodamine B (RhB) degradation in wastewater. In comparison to the pristine monomaterials, the results demonstrated that the heterojunction composites demonstrated excellent degradation and stability of RhB under ultrasonic circumstances. The existence of heterojunctions and the internal piezoelectric field created by ultrasonic driving work in concert to boost catalytic performance, and the organic dye's rate of degradation is further accelerated by the carriers that are mutually transferred between the composites., 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 © 2024 Elsevier Ltd. All rights reserved.)

The widespread usage of levofloxacin (LVF) intake is executed for several urinary and respiratory systems infections in human. But, its over intake leads to severe damage to humans and the environment by its exposure. Hence the detection of LVF is concerned and we herein developed an electrocatalyst, strontium tungsten oxide nanospheres and later decorated onto the functionalized multiwall carbon nanotubes (SrWO 4 /f-MWCNT) to perform effective electrochemical recognition of LVF in aquatic and biological samples. Binary metal oxide with carbon composite SrWO 4 /f-MWCNT was developed due to its specific features as nanostructures. Various methods of investigation have been examined to identify the physiochemical characteristics like X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and morphological characteristics including field emission scanning electron microscopy, and transmission electron microscopy. The synthesized SrWO 4 /f-MWCNT sample crystalline size was around 32.9 nm. The SrWO 4 /f-MWCNT modified glassy carbon electrode (GCE) has been subjected to electrochemical investigation with a wide linear range of 0.049 μM-574.73 μM with good sensitivity 2.86 μA μM -1 cm 2 , the limit of detection at 14.9 nM for LVF sensing. Furthermore, the designed LVF detection exhibited excellent anti-interference, stability, reproducibility, and repeatability. The as-developed sensor's electrochemical outcomes indicate the superior performance inherent in the developed composite., 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 © 2024 Elsevier Ltd. All rights reserved.)

In this study, we investigated the degradation of the flame retardant tetrabromobisphenol A (TBBPA) using platinized tungsten oxide (Pt/WO 3 ), synthesized via a simple photodeposition method, under visible light. The results of degradation experiments show a significant enhancement in TBBPA degradation upon surface platinization of WO 3 , with the degradation rate increasing by 13.4 times compared to bare WO 3 . The presence of Pt on the WO 3 surface stores conduction band electrons, which facilitates the two-electron reduction of oxygen and enhances the production of valence band holes (h VB + ) and hydroxyl radicals ( ● OH). Both h VB + and ● OH are significantly involved in the degradation of TBBPA in the visible light-irradiated Pt/WO 3 system. This was verified through fluorescence spectroscopy employing coumarin as a chemical probe and oxidizing species-quenching experiments. The analysis of degradation products and their toxicity assessment demonstrate that the toxicity of TBBPA-contaminated water is significantly reduced after Pt/WO 3 photocatalysis. The degradation rate of TBBPA increased with increasing Pt/WO 3 dosage, reached an optimum at a Pt content of 0.5 wt%, but decreased with increasing TBBPA concentration. The decrease in degradation efficiency of Pt/WO 3 was minor, both in the presence of various anions and after repeated use. This study proposes that Pt/WO 3 is a viable photocatalyst for the degradation of TBBPA in water under visible light., 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 © 2024 Elsevier Ltd. All rights reserved.)

Characterization and evaluation of hazardous spent V 2 O 5 -WO 3 /TiO 2 catalysts are critical to determining their treatment or final disposal. This study employs a thermal approach to simulate the preparation of spent catalysts derived from commercial V 2 O 5 -WO 3 /TiO 2 catalysts and investigate the structure-activity relationship of the carrier changes during the deactivation process. The results indicate that the catalyst carrier undergoes two processes: an increase in grain size and a transformation in crystal structure. Both structural and catalytic investigations demonstrate that the grain size for catalyst deactivation is 24.62 nm, and the formation of CaWO 4 occurs before the crystalline transformation. The specific surface area is susceptible to an increase in grain size. The reactions of selective catalytic reduction involve the participation of both Brønsted acid and Lewis acid sites. The deactivation process of the carrier initially affects Brønsted acid sites, followed by a reduction in Lewis acid sites, resulting in a decline in NH 3 adsorption capacity and oxidation. Correlation analysis reveals that changes in the physicochemical properties of the catalyst reduce the NO conversion, with the order being The grain size > Total acid amount > The surface area. It is recommended to recycle the spent catalyst if the carrier grain size is less than 25 nm. The findings of this investigation contribute to expanding the database for evaluating and understanding the physicochemical properties of spent catalysts for disposal., 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 © 2024 Elsevier Ltd. All rights reserved.)

In this study, the Fe(III)/WS 2 /peroxymonosulfate (PMS) system was found to remove up to 97% of cyclohexanecarboxylic acid (CHA) within 10 min. CHA is a model compound for naphthenic acids (NAs), which are prevalent in petroleum industrial wastewater. The addition of WS 2 effectively activated the Fe(III)/PMS system, significantly enhancing its ability to produce reactive oxidative species (ROS) for the oxidation of CHA. Further experimental results and characterization analyses demonstrated that the metallic element W(IV) in WS 2 could provide electrons for the direct reduction of Fe(III) to Fe(II), thus rapidly activating PMS and initiating a chain redox process to produce ROS (SO 4 •- , • OH, and 1 O 2 ). Repeated tests and practical exploratory experiments indicated that WS 2 exhibited excellent catalytic performance, reusability and anti-interference capacity, achieving efficient degradation of commercial NAs mixtures. Therefore, applying WS 2 to catalyze the Fe(III)/PMS system can overcome speed limitations and facilitate simple, economical engineering applications., 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 © 2024 Elsevier Ltd. All rights reserved.)

In recent years, the removal organic pollutants from wastewater by advanced oxidation processes, especially photocatalysis, has become a meaningful approach due to its eco-friendliness and low cost. Herein, staggered type-II Bi 2 WO 6 /WO 3 heterojunction photocatalysts were prepared by a facile hydrothermal route and investigated by modern physicochemical methods (X-ray diffraction, scanning electron microscopy, low-temperature nitrogen adsorption-desorption, and diffuse reflectance spectroscopy). The optimized BWOW-5 photocatalyst exhibited a H 2 O 2 -assisted photocatalytic methylene blue removal efficiency of 94.1% (k = 0.01414 min -1 ) within 180 min under optimal reaction conditions, which is much higher than that of unmodified Bi 2 WO 6 and WO 3 due to efficient separation of the photogenerated charge carriers. The trapping experiments demonstrated that photogenerated hydroxyl radicals and holes play a key role in the photodegradation reaction. Moreover, the optimized BWOW-5 heterojunction photocatalyst exhibited excellent activity in the H 2 O 2 -assisted degradation of other pollutants, namely phenol, isoniazid, levofloxacin, and dibenzothiophene with the removal rate of 63.1, 73.6, 95.0, and 72.4%, respectively. This investigation offers a design strategy for Bi 2 WO 6 -based multifunctional photocatalytic composites with improved activity for organic pollutant degradation., 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 © 2024 Elsevier Ltd. All rights reserved.)

Photocatalytic water purification has been extensively explored for its economic, eco-friendly, and sustainable aspects. In this study, tungsten (W) incorporated BaSn 1-x W x O 3 (x = 0 to 0.05) nanoparticles synthesized by facile hydrogen peroxide precipitation route has been demonstrated for photocatalytic degradation of methylene blue (MB) dye and ciprofloxacin (CIP) antibiotic. The structural analysis indicates the presence of hybrid composite-like nanostructures with reduced crystallinity. Optical studies reveal blueshift in bandgap and decrease in oxygen vacancy defects upon W-incorporation. Pure BaSnO 3 shows overall enhanced photocatalytic activity towards MB (90.22%) and CIP (78.12%) after 240 min of white LED light and sunlight irradiation respectively. The 2 % W-incorporated BaSnO 3 shows superior photocatalytic degradation of MB (26.89%) and CIP (45.14%) within first 30 min of irradiation confirming the presence of W to be beneficial in the process. The free radical study revealed the dominant role of reactive hole (h + ) and oxygen radical (O 2 •- ) species during photodegradation and their intermediates are investigated to elucidate the degradation mechanism of MB within 30 min of irradiation. This study is promising towards developing defect mediated and time-efficient photocatalysts for environmental remediation., 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 © 2024 Elsevier Ltd. All rights reserved.)

A co-precipitation technique has been used to prepare Bismuth tungstate nanoparticles (Bi 2 WO 6 ) for electrochemical capacitors and electrochemical sensing of Ascorbic acid (AA). Using a scanning rate of 10 mV s -1 , the electrode was performed as the pseudocapacitance behavior and the specific capacitance to be up to 677 Fg -1 at 1 A/g. Bi 2 WO 6 versus Glassy carbon electrode (GCE) was also used to study the behavior of the Bi 2 WO 6 modified electrodes in detecting ascorbic acid. This electrochemical sensor shows excellent electrocatalytic performance when ascorbic acid is present, as determined by differential pulse voltammetry. In solution, ascorbic acid diffuses to an electrode surface and controls its surface properties. Based on the results from the investigation, the sensor showed a detection sensitivity of 0.26 mM/mA, and a limit of detection (LOD) of 77.85 mM. It is clear from these results that Bi 2 WO 6 may find application as an electrode material for supercapacitors and glucose sensors., 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 © 2023 Elsevier Ltd. All rights reserved.)

In the present article, the disulfide tungsten/activated carbon derived from Eichhornia crassipes (WS 2 /AC) was synthesized by the hydrothermal process. The received materials were examined by X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray - mapping, and nitrogen adsorption/desorption isotherms. The morphology of WS 2 /AC was tailored to have a micro/meso/macro structure that facilized large electric conductivity and quick ion diffusion. The WS 2 /AC sample was used as an electrode modifier for developing an electrochemical sensor for salbutamol detection. WS 2 /AC exhibited excellent oxidation toward salbutamol. Through some optimized conditions, the electrochemical signal of the proposed sensor varied linearly to the salbutamol concentration ranging from 1 to 210 μM with a low LOD (detection limit) of 0.52 μM. The developed sensor showed several merits: easy producing, convenient usage, fabulous selectivity, and good repeatability as well as reproducibility. Finally, the suggested technique can be applied to determine salbutamol in people's biological fluid with satisfactory recoveries of 98.5-104.4% and without statistics different from standard HPLC., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The extensive use of pesticides for better yield of crops have become major human concern over the decades. Pesticides are widely used in the fields to kill weeds and pests on the vegetable and crops to improve the quality and yield of the food knowing the fact that pesticides residue in food are very lethal for human being. Amongst, the hazardous pesticides, mancozeb is widely applied in the protection of crops. Thus the quantification of mancozeb residue is of great importance. This study reports the electrochemical monitoring of mancozeb through tungsten oxide reduced graphene oxide (WO 3 /rGO) nanocomposite. The engineered nanocomposite was characterized though different analytical tools such as FTIR, XRD and TEM to examine crystallinity, internal texture and the size. The FTIR result confirm the functionalities of GO and WO 3 /rGO nanocomposite in finger print and functional group region. Through XRD analysis, the size of the WO 3 /rGO nanocomposite was calculated as 31.6 nm. While the TEM analysis was also exploited to examine the 2D texture of GO and nanometric size of the WO 3 /rGO. To ensure the conductive nature of the WO 3 /rGO nanocomposite, the glassy carbon electrode was modified and exploited for cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Under the optimal conditions, the modified sensor showed exceptional response for mancozeb. The linear dynamic range was set from 0.05 to 70 μM in BRB buffer of pH 4. The LOD and LOQ for proposed method was calculated as 0.0038 and 0.0115 μM. The analytical applicability of chemically modified sensor was investigated in real matrix of different vegetable samples and the recovery values were observed in acceptable range. The electrochemical examination of present work reveals that WO 3 /rGO nanocomposite can be an exceptional aspirant for the determination of mancozeb at commercial level., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Due to the multi-catalysis of the WO 3 and excellent properties of the graphene (GO), a series of rGO-WO 3 nanocomposites were prepared through the hydrothermal synthesis procedure by changing the material ratio, the reaction temperature and the reaction time in this paper, and then added it into a dielectric barrier discharge plasma (DBDP) system for investigating the bisphenol A (BPA)'s degradation and corresponding catalytic mechanism of the rGO-WO 3 in the DBDP system. The obtained results show that there was an optimum dosage of the rGO-WO 3 (40 mg/L) as well as the preparation conditions (5:1000 mass ratio of the GO and the WO 3 , 18 h reaction time and 120 °C reaction temperature) for achieving the highest catalytic effect, and the highest degradation rate constant of the BPA was 0.03129 min -1 . The determined higher TOC removal, higher COD removal as well as UV-Vis analysis also demonstrated the catalysis of the rGO-WO 3 . The measurement of the change of the O 3 and the H 2 O 2 concentrations in the reaction system with or without the rGO-WO 3 and with or without the BPA proved the catalysis of the rGO-WO 3 on the ·OH formation, while the combination of the GO had the positive effect for enhancing the catalytic effect. A figure on the catalysis and degradation procedure of the BPA in the DBDP/rGO-WO 3 system was provided in the paper., 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.)

Tungsten (W) occurrence and speciation was investigated in sediments collected from Fallon, Nevada where previous studies have linked elevated W levels in human body fluids to an unusual cluster of childhood leukemia cases. The speciation of sedimentary W was determined by μ-XRF mapping and μ-XANES. The W content of the analyzed surface sediments ranged between 81 and 25,908 mg/kg, which is significantly higher than the W content in deeper sediments which ranged from 37 to 373 mg/kg at 30 cm depth. The μ-XANES findings reveal that approximately 20-50% of the total W in the shallow sediment occurs in the metallic form (W 0 ); the rest occurs in the oxide form (W VI O 3 ). Because W 0 does not occur naturally, its elevated concentrations in surface sediments point toward a possible local anthropogenic origin. The oxidation of metallic W 0 with meteoric waters likely leads to the formation of W VI O 3 . The chief water-soluble W species was identified as WO 4 2- by chromatographic separation and speciation modeling. These results led us to postulate that W 0 particles from a currently unknown but local source(s) is (are) deposited onto the soils and/or surface sediments. The W 0 in interaction with meteoric water is oxidized to W VI O 3 , and as these sediment-water interactions progress, WO 4 2- is formed in the water at pH ∼7. Under pH < 7, and sufficient W concentrations, tungstate tends to polymerize, and polymerized species are less likely to adsorb onto sediments. Polymerized species have lower affinity than monomers, which leads to enhanced mobility of W., 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 effect of trace metals, namely tungsten and selenium, on the production of acids and alcohols through gas fermentation by a CO-enriched anaerobic sludge in a continuous gas-fed bioreactor was investigated. The CO-enriched sludge was first supplied with a tungsten-deficient medium (containing selenium) and in a next assay, a selenium-deficient medium (containing tungsten) was fed to the bioreactor, at a CO gas flow rate of 10 mL/min. In the absence of tungsten (tungstate), an initial pH of 6.2 followed by a pH decrease to 4.9 yielded 7.34 g/L acetic acid as the major acid during the high pH period. Subsequently, bioconversion of the acids at a lower pH of 4.9 yielded only 1.85 g/L ethanol and 1.2 g/L butanol in the absence of tungsten (tungstate). A similar follow up assay in the same bioreactor with two consecutive periods at different pH values (i.e., 6.2 and 4.9) with a selenium deficient medium yielded 6.6 g/L acetic acid at pH 6.2 and 4 g/L ethanol as well as 1.88 g/L butanol at pH 4.9. The results from the microbial community analysis showed that the only known CO fixing microorganism able to produce alcohols detected in the bioreactor was Clostridium autoethanogenum, both in the tungsten and the selenium deprived media, although that species has so far not been reported to be able to produce butanol. No other solventogenic acetogen was detected., Competing Interests: Declarations of competing interest None., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

In this study, WO 3 nanostructures were synthesized by the electrochemical anodization technique to use them on the degradation of persistent organic compounds such as the pesticide fenamiphos. The acids electrolyte used during the anodization were two different: 1.5 M H 2 SO 4 - 0.05 M H 2 O 2 and 1.5 M CH 4 O 3 S - 0.05 M H 2 O 2 . Once the samples have been manufactured, they have been subjected to different tests to analyze the properties of the nanostructures. With Field Emission Scanning Electron Microscopy (FE-SEM) the samples have been examined morphologically, their composition and crystallinity has been studied through Raman Spectroscopy and their photoelectrochemical behaviour by Photoelectrochemical Impedance Spectroscopy (PEIS). Finally, degradation tests have been carried out using the technique known as photoelectrocatalysis (PEC). The conditions that were applied in this technique were a potential of 1 V Ag/AgCl and simulated solar illumination. The degradation process was monitored by UV-Visible and High-Performance liquid Chromatography (HPLC) to control the course of the experiment. The nanostructures obtained with 1.5 M CH 4 O 3 S - 0.05 M H 2 O 2 electrolyte showed a better photoelectrochemical behaviour than nanostructures synthesized with 1.5 M H 2 SO 4 - 0.05 M H 2 O 2 . The fenamiphos degradation was achieved at 2 h of experiment and the intermediate formation was noticed at 1 h of PEC experiment., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Pulsed discharge plasma (PDP) was adopted to induce WO 3 for synergetic degradation of ciprofloxacin (CIP) in water. WO 3 was firstly characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller (BET), X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS), Photocurrents and Photoluminescence. The degradation results showed that PDP could induce WO 3 photocatalysis successfully, and a synergetic effect was established in PDP/WO 3 system. After 60 min treatment time, 0.16 g/L WO 3 increased the CIP removal from 71.3% to 99.6%, with the enhancement of the first-order kinetic constant from 0.020 min -1 to 0.081 min -1 . Then, the effect of peak voltage, air flow rate and pH on CIP removal was evaluated. Active species trapping test verified that ·OH and ·O 2 - played the major role for plasma-degradation of CIP degradation, whereas OH and h + were conductive to catalytic degrade CIP. WO 3 addition lead to the decline of O 3 and enhancement of OH no matter in deionized water or CIP solution. The degradation process was explored using fluorescence spectrograph, liquid chromatography-mass spectrometry (LC-MS) and ion chromatography (IC). Finally, the possible degradation pathways of CIP degradation were proposed. The reuse test suggested WO 3 possessed excellent catalytic performance as well as good stability., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

As a carcinogenic byproduct in drinking water treatment, bromate has raised global concerns on environmental and health hazard, calling for effective treatments. In the current work, a novel reduced graphene oxide supported polyaniline/WO 2.72 nanobelt-flower (RGO/PANI/WO 2.72 ) ternary composite was prepared through a solvent volatilization method for photocatalytic reduction of bromate. The prepared sample was characterized, and the influence of aqueous pH, ions and dissolved oxygen on the bromate reduction was explored. As expected, the introduction of RGO and PANI on the WO 2.72 exhibited great synergistic effects on the separation of photogenerated carriers. The calculated reduction rate constant of RGO/PANI/WO 2.72 was about six times as high as that of pure WO 2.72 . Specially, the prepared photocatalyst possessed strong optical absorption in a broad range of 250-2500 nm, and thus displaying excellent catalytic performance in utilization of all solar spectrum energy. Moreover, the RGO/PANI/WO 2.72 exhibited stable photocatalytic activity in cycling test. Considered holistically, the present study offered a valuable approach for rational construction of heterogeneous structure in the development of bromate-catalyzed reduction., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Ammonia (NH 3 ), is a precursor for the formation of atmospheric fine particulate matter (PM 2.5 ), and thus establishing efficient and cost-effective methods to detect ammonia emission is highly desired. Transition metal oxide semiconductors-based sensors for electrochemical gas sensing have been extensively explored. Among various types of semiconductors, tungsten oxide (WO 3 ) possesses an anisotropic layered crystalline structure and is recognized as a promising material for gas sensing. However, the performance of commercial WO 3 is unsatisfactory because of its high impedance and low charge transportation efficiency. Thus, the modification of commercial WO 3 is needed to make it an efficient ammonia sensor material. In this work, closely packed WO 3 microspheres with oxygen vacancies were synthesized successfully through a novel two-step hydrothermal route. Our WO 3 showed a good selectivity to ammonia sensing, and its response intensity was 2.6 times higher than that of commercial WO 3 because of its optimized conductivity. Moreover, the mechanism behind its robust ammonia sensing performance was elucidated. The effectiveness of the as-prepared WO 3 microspheres for ammonia sensing also suggests a new strategy for modifying transition metal oxide materials., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Photocatalytic nanoparticles have been receiving considerable attention for their potential use in many environmental management applications, including urban air quality control. This paper investigates the performance of surface modified WO 3 /TiO 2 composite particles in removing gaseous nitrogen oxides (NO x ) under visible light irradiation. The WO 3 /TiO 2 composite particles were synthesized using a modified wet chemical method with different concentrations of NaOH solution used as a surface modification agent for the host TiO 2 particles. The NO x removal efficiency of the WO 3 /TiO 2 particles was evaluated using a lab-scale continuous gas flow photo-reactor with a gas contact time of 1 min. Results showed that surface modification using NaOH can enhance the photocatalytic activity of the WO 3 /TiO 2 particles. The NO x removal efficiency of the surface modified WO 3 /TiO 2 was greater than 90%, while that of WO 3 /TiO 2 particles prepared by the conventional wet chemical method was ∼75%. The enhanced removal efficiency might be attributed to the formation of oxygen vacancies on the TiO 2 surface, providing sites for WO 3 particles to effectively bind with TiO 2 . However, excess amount of NaOH >3 M deteriorated the photocatalytic performance due to the increased agglomeration of the host TiO 2 particles., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

Photochemical decomposition of a fluorotelomer unsaturated carboxylic acid, C3F7CFCHCOOH (1), in the presence of WO3 and an electron acceptor (S2O8(2-) or H2O2) in water under visible-light irradiation was investigated. Under an O2 atmosphere, 1 was not decomposed either by TiO2 (P25) or WO3 alone. A combination of WO3 and H2O2 also resulted in almost no decomposition of 1. In contrast, irradiation in the presence of a combination of WO3 and S2O8(2-) (potassium salt) efficiently decomposed 1 to F(-), CO2, C3F7COOH, and C2F5COOH. The decomposition of 1 was affected by the counter cation of S2O8(2-): the decomposition extent was higher with K2S2O8 than with (NH4)2S2O8. The decomposition of 1 was further enhanced when the reaction in the presence of WO3 and K2S2O8 was carried out under an argon atmosphere. Under O2, the amount of H2O2 formed in the reaction solution was an order of magnitude higher than the amount formed under argon. This fact suggests that the decrease in the decomposition of 1 under O2 can be ascribed to the formation of H2O2, which consumed S2O8(2-) and SO4(-)., (Copyright © 2013 Elsevier Ltd. All rights reserved.)

New assays with HepG2 cells indicate that Indigo Carmine (IC), a dye that is widely used as additive in many food and pharmaceutical industries exhibited cytotoxic effects. This work describes the development of a bicomponent nanostructured Ti/TiO2/WO3 electrode prepared by "template" method and investigates its efficiency in a photoelectrocatalytic method by using visible light irradiation and applied potential of 1V. After 2h of treatment there are reduction of 97% discoloration, 62% of mineralization and formation of three byproducts assigned as: 2-amine-5-sulfo-benzoic acid, 2,3-dioxo-14-indole-5-sulfonic acid, and 2-amino-α-oxo-5-sulfo-benzeneacetic acid were identified by HPLC-MS/MS. But, cytotoxicity was completely removed after 120 min of treatment., (Copyright © 2013 Elsevier Ltd. All rights reserved.)

Pentachlorobenzene (PeCB) in simulated flue gas was destructed by a commercial V(2)O(5)-WO(3)/TiO(2) catalyst in this study. The effects of reaction temperature, oxygen concentration, space velocity and some co-existing pollutants on PeCB conversion were investigated. Furthermore, a possible mechanism for the oxidation of PeCB over the vanadium oxide on the catalysts was proposed. Results show that the increase of gas hourly space velocity (GHSV) and the decrease of operating temperature both resulted in the decrease of PeCB removal over the catalyst, while the effect of the oxygen content in the range of 5-20% (v/v) on PeCB conversion was negligible. PeCB decomposition could be obviously affected by the denitration reactions under the conditions because of the positive effect of NO but negative effect of NH(3). The introduction of SO(2) caused the catalyst poisoning, probably due to the sulfur-containing species formed and deposited on the catalyst surface. The PeCB molecules were first adsorbed on the catalyst surface, and then oxidized into the non-aromatic acyclic intermediates, low chlorinated aromatics and maleic anhydride., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

A comprehensive study of the degradation of monuron, one of the phenylurea herbicides, was conducted by UV-Vis/WO(3) process. It was found that hydroxyl radicals played a major role in the decay of monuron while other radicals (e.g. superoxide) and hole might also contribute to the decomposition of monuron. The oxidation path likely plays a major role in the generation of hydroxyl radicals. The effects of initial pH level, initial concentration of monuron, and inorganic oxidants on the performance of UV-Vis/WO(3) process were also investigated and optimized. Comparison between monuron decay pathways by UV-Vis/WO(3) and UV/TiO(2) was conducted. The decay mechanisms, including N-terminus demethylation, dechlorination and direct hydroxylation on benzene ring, were observed to be involved in the oxidation of monuron in these two processes. Sixteen intermediates were identified during the photodegradation of monuron and degradation pathways were proposed accordingly., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

This study investigates the dissolution, sorption, leachability, and plant uptake of tungsten and alloying metals from canister round munitions in the presence of model, well characterized soils. The source of tungsten was canister round munitions, composed mainly of tungsten (95%) with iron and nickel making up the remaining fraction. Three soils were chosen for the lysimeter studies while four model soils were selected for the adsorption studies. Lysimeter soils were representatives of the typical range of soils across the continental USA; muck-peat, clay-loamy and sandy-quartzose soil. Adsorption equilibrium data on the four model soils were modeled with Langmuir and linear isotherms and the model parameters were obtained. The adsorption affinity of soils for tungsten follows the order: Pahokee peat>kaolinite>montmorillonite>illite. A canister round munition dissolution study was also performed. After 24 d, the measured dissolved concentrations were: 61.97, 3.56, 15.83 mg L(-1) for tungsten, iron and nickel, respectively. Lysimeter transport studies show muck peat and sandy quartzose soils having higher tungsten concentration, up to 150 mg kg(-1) in the upper layers of the lysimeters and a sharp decline with depth suggesting strong retardation processes along the soil profile. The concentrations of tungsten, iron and nickel in soil lysimeter effluents were very low in terms of posing any environmental concern; although no regulatory limits have been established for tungsten in natural waters. The substantial uptake of tungsten and nickel by ryegrass after 120 d of exposure to soils containing canister round munition suggests the possibility of tungsten and nickel entering the food chain., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

We studied the bacterial diversity at a single location (the Terrubias mine; Salamanca province, Spain) with a gradient of soil As contamination to test if increasing levels of As would (1) change the preponderant groups of arsenic-resistant bacteria and (2) increase the tolerance thresholds to arsenite [As(III)] and arsenate [As(V)] of such bacteria. We studied the genetic and taxonomic diversity of culturable arsenic-resistant bacteria by PCR fingerprinting techniques and 16S rRNA gene sequencing. Then, the tolerance thresholds to As(III) and As(V) were determined for representative strains and mathematically analyzed to determine relationships between tolerances to As(III) and As(V), as well as these tolerances with the soil contamination level. The diversity of the bacterial community was, as expected, inversely related to the soil As content. The overall preponderant arsenic-resistant bacteria were Firmicutes (mainly Bacillus spp.) followed by γ-Proteobacteria (mainly Pseudomonas spp.), with increasing relative frequencies of the former as the soil arsenic concentration increased. Moreover, a strain of the species Rahnella aquatilis (γ-Proteobacteria class) exhibited strong endurance to arsenic, being described for the first time in literature such a phenotype within this bacterial species. Tolerances of the isolates to As(III) and As(V) were correlated but not with their origin (soil contamination level). Most of the strains (64%) showed relatively low tolerances to As(III) and As(V), but the second most numerous group of isolates (19%) showed increased tolerance to As(III) rather than to As(V), even though the As(V) anion is the prevalent arsenic species in soil solution at this location. To our knowledge, this is the first study to report a shift towards preponderance of Gram-positive bacteria (Firmicutes) related to high concentrations of soil arsenic. It was also shown that, under aerobic conditions, strains with relatively enhanced tolerance to As(III) predominated over the most As(V)-tolerant ones., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

Physical changes that occur on the surface of fired shots due to firing and impact with soil may increase the dissolution of muniton metals. Increased metal dissolution could potentially increase metal transport and leaching, affecting metal concentrations in surface and groundwater. This research describes the relationship between the surface changes on fired tungsten-nickel-iron (94% W:2% Ni:4% Fe) composite shots and metals leaching from those shots. Tungsten composite shot was fired into, and aged in, three soil types (Silty Sand, Sandy Clay, and Silt) in mesoscale rainfall lysimeters to simulate live-fire conditions and subsequent interactions between the metals of the composite and soil. Leachate, runoff, and soil samples were collected from the lysimeters and analyzed for metal content. The shots were analyzed using scanning electron microscopy (SEM) to evaluate surface changes. SEM results indicated that a soil's particle size distribution initially affected the amount of metal that was sheared from the surface of the fired W-composite shots. Shearing was greatest in soils with larger soil particles (sand and gravel); shearing was least in soils composed of small soil particles (fines). Increased metallic shearing from the shot's surface was associated with increased W dissolution, compared to controls, following a simulated 1 year soil aging., (Published by Elsevier Ltd.)

The decomposition of hydroperfluorocarboxylic acids [H-PFCAs; HC(n)F(2)(n)COOH (n=4 and 6)] induced by heteropolyacid photocatalyst H(4)SiW(12)O(40) in water was investigated, and the results are compared with the results for the corresponding perfluorocarboxylic acids (PFCAs; C(n)F(2)(n)(+1)COOH). This is the first report on the photochemical decomposition of H-PFCAs, which are being developed as alternative surfactants to environmentally persistent and bioaccumulative PFCAs. H-PFCAs were not decomposed by irradiation with UV-Visible light (>290 nm) in the absence of H(4)SiW(12)O(40). In contrast, UV-Visible light irradiation of H-PFCAs in the presence of H(4)SiW(12)O(40) efficiently decomposed H-PFCAs to F(-) and CO(2). The decomposition reactions showed pseudo-first-order kinetics, and the decomposition rate constants were 1.8-2.5 times higher than those for the corresponding PFCAs. The reaction mechanism can be explained by elimination of H(+) from the ω-H atom of the H-PFCAs by the excited catalyst, followed by formation of perfluorodicarboxylic acids., (Copyright © 2010 Elsevier Ltd. All rights reserved.)

Development of effective PCDD/F (polychlorinated dibenzo-p-dioxin and dibenzofuran) control technologies is essential for environmental engineers and researchers. In this study, a PCDD/F-containing gas stream generating system was developed to investigate the efficiency and effectiveness of innovative PCDD/F control technologies. The system designed and constructed can stably generate the gas stream with the PCDD/F concentration ranging from 1.0 to 100ng TEQ Nm(-3) while reproducibility test indicates that the PCDD/F recovery efficiencies are between 93% and 112%. This new PCDD/F-containing gas stream generating device is first applied in the investigation of the catalytic PCDD/F control technology. The catalytic decomposition of PCDD/Fs was evaluated with two types of commercial V(2)O(5)-WO(3)/TiO(2)-based catalysts (catalyst A and catalyst B) at controlled temperature, water vapor content, and space velocity. 84% and 91% PCDD/F destruction efficiencies are achieved with catalysts A and B, respectively, at 280 degrees C with the space velocity of 5000h(-1). The results also indicate that the presence of water vapor inhibits PCDD/F decomposition due to its competition with PCDD/F molecules for adsorption on the active vanadia sites for both catalysts. In addition, this study combined integral reaction and Mars-Van Krevelen model to calculate the activation energies of OCDD and OCDF decomposition. The activation energies of OCDD and OCDF decomposition via catalysis are calculated as 24.8kJmol(-1) and 25.2kJmol(-1), respectively.

WO(3) and Zn-doped WO(3) thin films were prepared on indium-tin oxide glass by a dip-coating. The composite films were characterized by UV-Vis absorption spectra, X-ray diffraction and scanning electron microscope. The effect of preparation conditions (concentration of Zn, annealing temperature, number of layers) on the photocurrent was studied. It was found that the photocurrent under visible light displayed the highest value for 2% Zn-WO(3) films annealed at 400 degrees C. The photocatalytic activity of the Zn-doped WO(3) was evaluated in terms of decay rate of nitrite ions under visible light. The influence of applied potential, initial pH and nitrite concentration on the reaction rate was studied. The experiments demonstrated that NO(2)(-) could be efficiently degraded on the doped photoanode that showed a higher activity than the undoped WO(3) especially under high anodic potential (>0.7 V). The rate of degradation was enhanced in aqueous NaCl solutions. Furthermore, it was demonstrated that the photodegradation mechanism of NO(2)(-) proceeded mainly indirectly via OH radicals. The possible reason of enhancement of reaction rate was also discussed.

Studies on the catalytic destruction of 1,2-dichlorobenzene were carried out on a specially constructed semi-technical equipment whose most important element was a catalytic reactor with a monolithic catalyst in the form of 150 x 150 x 100 mm cubes. A catalyst made from cordierite with an active layer composed of Al2O3 - 64 wt%, TiO2 - 26 wt%, V2O5 - 6.6 wt% and WO3 - 3.4 wt% was used. The reactor made it possible to carry out the process in the temperature range 150-350 degrees C, at variable catalyst loading and different velocities of gas flow through the reactor. The content of 1,2-dichlorobenzene in the air was analysed by a chromatographic method. A significant effect of catalyst loading and temperature on 1,2-dichlorobenzene destruction efficiency was observed and no effect of the linear flow velocity through the catalyst on o-dichlorobenzene destruction efficiency was reported. The applied vanadium-tungsten catalyst on a monolithic carrier made from TiO2/gamma-Al2O3 revealed very good activity that resulted in an over 80% efficiency of 1,2-dichlorobenzene destruction at the temperature around 250 degrees C at a very high catalyst loading reaching ca. 8200 h(-1). Additionally, in this study the kinetics of 1,2-dichlorobenzene decomposition was determined, specifying the order of reaction and dependence of the decomposition rate constant on temperature, using a simple power-rate law model.

Tungsten trioxide thin films on transparent substrates (glass and F:SnO(2) or ITO-coated glass) were prepared by layer-by-layer brush painting and spin-coating using organic precursors. Well-crystallized WO(3) with monoclinic structure was formed on all substrates after annealing at 500 degrees C or above. The dense semiconducting films are specular and transparent outside the band-gap. Their photoactivity in junctions with aqueous electrolytes extends up to 470 nm, with incident photon to current conversion efficiencies around 0.9 at 313 nm and up to 0.1 at 436 nm. Films of 10 cm x 10 cm were used for the study of solute degradation reactions in a thin-film reactor under backside illumination. Dilute aqueous solutions of model substances for contaminants like oxalic acid were decomposed under continuous flow using broadband UVA illumination and electrical bias. Operation under solar illumination was also feasible. The advantage over operation without bias (conventional photocatalysis) prevailed for all decomposition reactions studied.