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AbstractFood dyes with a diverse set of colorants stimulate appetite and enhance aesthetic charm of food on table but at the same time these dyes contaminate the aquatic and biological ecosystems due to their cytotoxic and carcinogenic potentials. Herein, we report magnetite catalyzed removal of sunset yellow dye from water through catalytic degradation and ozonation. The magnetite catalyst revealed about 83% catalytic degradation and 92% catalytic ozonation performance toward sunset yellow dye at 100 and 25 min, respectively. Furthermore, the persulphate/magnetite/O3 hybrid system revealed superior performance compared to the persulphate/magnetite under identical conditions. Kinetic studies revealed that the dye degradation data followed second-order kinetics, suggesting that the dye removal process is physicochemical in nature. This study further demonstrates that the persulfate/magnetite/O3 hybrid system can efficiently decompose sunset yellow dye in aqueous solution compared to the Fenton’s reagent and simple catalytic decomposition processes which is attributed to its unique structural features.

AbstractElectrochromic (EC) thin films have received considerable attention due to their potential applications in various fields such as smart windows, electrochromic displays, and energy storage devices. This review highlights various methods used for the fabrication and functionalization of EC films for various applications. Various techniques for EC thin film deposition ranging from solution-processable, low-temperature approaches such as sol-gel, spin coating, dip coating, and spray pyrolysis, to advanced techniques for deposition such as physical vapor deposition, chemical vapor deposition, and sputtering are summarized in this review. In addition, various applications of EC thin films and the outcome of different deposition approaches on the opto-electrochromic properties of EC thin films have been discussed elaborately. This review has the potential to spark the interest of researchers from a broad range of disciplines, including photocatalysis, electrocatalysis, nanotechnology and materials science.

In recent years, green nanomaterials are increasingly being utilized in horticulture and agriculture due to their potential to transform plant development, improve crop yield, combat diseases, and pest management, among other applications. Significantly, green nanomaterials enhance nutrient delivery by improving stability, uptake, and solubility efficiency. Utilizing non-toxic precursors, waste reduction strategies, renewable resources, and energy-efficient processes, they offer sustainable technology advancement. Moreover, tomatoes, the largest domestic and industrial crop, yield around 200 million tons globally. They are beneficial for blood cleansing, gastrointestinal secretion, and nutrient reduction. However, they are susceptible to diseases like early blight, septoria leaf spot, late blight, and buckeye rot. In this regard, green nanomaterials have the potential to revolutionize agriculture by improving disease management, detecting diseases quickly, enhancing nutrient uptake, safely delivering agrochemicals, and reducing pesticide dosage. So, impressed by this, in this current review paper, we explored the use of green nanomaterials for tomato growth, and development and investigated their unique features, utilization, challenges, and future prospects. Ultimately, this review will open a new research gateway for plant-based nanomaterial and their utilization in various disciplines particularly for crop protection, growth, and soil health.

This work aims to explore the efficiency of ZnO nanoparticles synthesized via the non-thermal gliding arc discharge-assisted plasma (NT-GAD) technique for inhibiting the corrosion of X60 API 5L steel in a 1M HCl environment. The XRD pattern revealed that the ZnO nanoparticles exhibit hexagonal wurtzite structure with average particle size of ∼24 nm. UV–visible spectroscopy analysis revealed an absorption peak centering at 365 nm, corresponding to an energy band gap of 3.29 eV. SEM and TEM analysis revealed that the nanoparticles exhibit an agglomerated and irregular morphology. The corrosion inhibition of ZnO NPs was investigated via the electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization tests (PDP), while varying both concentration and temperature. The results revealed that the increase in inhibitor concentration resulted in a higher activity at ambient temperature, with an optimal efficiency of 93 % at a concentration of 100 mg/L. However, the increase in temperature remarkably reduced the inhibition efficiency, suggesting a physisorption behavior of ZnO NPs onto the steel surface. AFM and FE-SEM analysis confirmed the formation of a protective layer on the X60 API 5L steel surface. This study emphasizes the significant potential of ZnO NPs synthesized via the NT-GAD assisted plasma technique as corrosion inhibitor for X60 API 5L carbon steel in 1M HCl corrosive media.

Inflammation coupled with oxidative stress contribute to the pathogenicity of various clinical disorders. Oxidative stress arises from an imbalance between production of reactive oxygen species (ROS) and antioxidant defense system, leading to cellular damages. The study investigated the antioxidant and anti-inflammatory effects of polysaccharides isolated from Lepidium sativum seed-coat mucilage. The water-soluble polysaccharides were extracted from mucilage and fractionated using gel permeation chromatography. The radical scavenging potential of various fractions was determined using DPPH, H2O2, and lipid peroxidation assays. The most effective EC50 was recorded for F53 (57.41 ± 1.34 μg/mL), followed by F20 (69.19 ± 0.61 μg/mL) and F52 (75.06 ± 0.45 μg/mL). In vitro anti-inflammatory effect was determined through human membrane stabilization assay while the in vivo effect was evaluated using a carrageenan-induced paw edema in mouse model where F53 demonstrated significant (P = 0.05) anti-inflammatory potential (92.60 % compared to diclofenac sodium 91.46 %). GC-MS analysis revealed the presence of galacturonic acid and glucuronic acid as main acidic monosaccharides along with varying quantities of rhamnose, arabinose, and maltose as prominent neutral monosaccharides. The study concludes that cress seed mucilage contains potent antioxidant and anti-inflammatory polysaccharides. Further studies on the mode of action of these polysaccharides could provide deeper insights into their potential use as antioxidant and anti-inflammatory agents.

Biochar is a porous, high-surface-area, black carbon-rich product that offers a cost-effective and environmentally friendly option to replace conventional charcoal. However, its specific structure and limited biodegradability pose challenges for its widespread applications. Photocatalysis is suggested as an alternative approach to harness solar energy and transform it into solar fuels. Interestingly, nanomaterials-based photocatalysts with tailored energy band properties and non-toxic characteristics, high surface areas, enhanced stability, and tunable pore sizes, have gained attention for their potential in diverse applications. Therefore, existing research on biochar-based photocatalysis systems (BBPs) aims to address different environmental issues. Interestingly, BBPs offer benefits such as excellent electrical conductivity, versatile functional groups, large surface area, and multiple surface-active sites, promoting high charge mobility, electron reservoir, superior charge separation, and small bandgap. This review provides a comprehensive overview of BBPs developments, including synthesis methods and properties. The fusion of BBPs is used in CO2 conversion, photocatalytic H2 generation, CO2 reduction, pollutants, dyes, and pharmaceutical degradation. Although the intermarriage of BBPs has potential benefits, their effectiveness may be compromised when modified photocatalysts are incorporated, which may negatively influence carrier generation efficiency and overall performance. Therefore, there is empty room for further research on their physical properties, effectiveness, long-term stability, and reusability of BBPs.

Effective wastewater treatment is essential due to the dye environmental threats. Photocatalysis offers an eco-friendly dye degradation solution. Herein, we report a double Z-scheme photocatalyst, i.e. LaFeO3/Boron-doped g-C3N4/Fe2O3 (LFO/B-CN/FO), fabricated via a hydrothermal method. The formation of this ternary system is supported by structural, surface, and morphological analyses. Differential scanning calorimetry and thermal gravimetric analysis demonstrated the crystallization behavior of the composite. Because of synergetic effects in the ternary composite and boron doping, the optical band gap energy is reduced to 1.6 eV. Under visible light irradiation, the LFO/B-CN/FO nanocomposite degraded navy-blue dye by 98% in 130 min at neutral pH, surpassing CN, B-CN, and binary composites of B-CN with LFO and FO. The degradation process was rationalized using pseudo-first- and pseudo-second-order kinetic models, which confirmed high catalytic efficiency. The double Z-scheme heterojunction enhanced light absorption, charge separation, and carrier lifetime, hence improving the photocatalytic activity. Overall, the as-fabricated LFO/B-CN/FO ternary composite outperformed reference catalysts in terms of chemical reactivity, optical characteristics, and electrical performance. This work opens up a new route for the design and fabrication of double Z-scheme ternary composite photocatalysts for potential wastewater treatment and renewable energy applications.

ABSTRACTThe growing demand for renewable energy sources has driven research efforts towards highly efficient electrochemical processes, especially the Hydrogen Evolution Reaction (HER) which is an essential component in renewable hydrogen production. Single Atom Catalysts (SACs) have been recognised as promising catalysts for exceptional HER activities owing to their unique electronic and geometrical features. This comprehensive review highlights the effective correlation between computational modelling and experimental research in fabricating new SACs and better understanding their catalytic mechanisms in the HER. Furthermore, the review briefly describes the choice of metals and tailoring the electronic structure, as well as exploring the influence of the reaction parameters on the catalytic activity of SACs for HER. Concluding remarks alongside future perspectives on the improvement of SACs for HER are emphasised. It is hoped that this review will pave the way for rational design of highly effective, low-cost and stable SACs for sustainable hydrogen production.

ABSTRACTThe quality of water significantly affects the health and walefare of all orginisms, highlighting the importance to develop low-cost and efficient wastewater treatment methods. Herein, we report the fabrication, characterization, and utilization of a polymer-based ternary nanocomposite (CuO–SiO2/PVA) for the removal of Nile Blue (NB) and Methylene Blue (MB) contaminants from wastewater, along with exploring its potential biological activities. We have successfully employed the cost-effective sol–gel and in-situ polymerization approaches to fabricate the CuO–SiO2/PVA based ternary composite, utilizing Cu(NO3)2·3H2O:Glycerol:TEOS:PVA in a ratio of 8:2:3:4. The desired fabrication of nanocomposite was confirmed through UV-Visible spectroscopy, SEM (scanning electron microscope), TEM (transmission electron microscope), EDX (energy dispersive X-ray diffraction), FTIR (Fourier transform infrared), DSC (differential scanning calorimetry), and TGA (thermogravimetric analysis). In addition to its biological potentialthe performance of the nanocomposite in catalytic / photocatalytic removal of NB and MB dyes is investigated and compared. The higher photodegradation performance of the composite for NB (85%) dye than for MB (76%) dye indicates that variables such as chemical structure, charge, molecular mass, and pH sensitivity of the dyes can influence the catalyst's removal potential. This composite is considered to have a higher capability for removing pollutants and microorganisms from wastewater.

This review underscores the fundamentals of MIP-CMs and systematically summarizes their synthetic strategies and applications, and potential developments. MIP-CMs are widely acclaimed for their versatility, finding applications in separation, filtration, detection, and trace analysis, as well as serving as scaffolds in a range of analytical, biomedical and industrial contexts. Also characterized by extraordinary selectivity, remarkable sensitivity, and outstanding capability to bind molecules, those membranes are also cost-effective, highly stable, and configurable in terms of recognition and, therefore, inalienable in various application fields. Issues relating to the potential future for the paper are discussed in the last section with the focus on the improvement of resource practical application across different areas. Hence, this review can be seen as a kind of cookbook for the design and fabrication of MIP-CMs with an intention to expand the scope of their application.

Bakanae is one of the important diseases of rice in Bangladesh that causes substantial yield loss every year. We collected thirty isolates of Fusarium spp. from bakanae-infected rice plants from different agroecological zones of Bangladesh and investigated the variations in cultural and morphological characteristics and pathogenicity. Diversity was found in cultural characteristics, viz., colony features, phialide, chlamydospore formation, shape, and size of macro- and microconidia. Three variants of Fusarium species such as F. moniliforme, F. fujikuroi, and F. proliferatum were identified on PDA media based on their cultural and morphological characteristics. Isolate FM10 (F. moniliforme) exhibited the highest disease aggressiveness in developing elongated plants (26.50 cm), the highest number of chlorotic leaves (5.75), and a lower germination percentage. We evaluated different bioagents against the virulent isolate of F. moniliforme to develop a rice bakanae disease management approach. Four bioagents, viz., Trichoderma spp., Bacillus subtilis, Pseudomonas fluorescens, and Achromobacter spp., were evaluated for growth suppression of F. moniliforme. Among the bioagents, Achromobacter spp. and B. subtilis (BS21) showed 73.54% and 71.61% growth suppression, respectively. The investigation revealed that the application of Achromobacter spp. and B. subtilis (BS21) would be a potential candidate for effective and eco-friendly management of the bakanae disease of rice.

Modern industries rapid expansion has heightened energy needs and accelerated fossil fuel depletion, contributing to global warming. Additionally, organic pollutants present substantial risks to aquatic ecosystems due to their stability, insolubility, and non-biodegradability. Scientists are currently researching high-performance materials to address these issues. LaFeO3 nanosheets (LFO-NS) were synthesized in this study using a solvothermal method with polyvinylpyrrolidone (PVP) as a soft template. The LFO-NS demonstrate superior performance, large surface area and charge separation than that of LaFeO3 nanoparticles (LFO-NP). The LFO-NS performance is further upgraded by incorporating ZIF-67. Our results confirmed the ZIF-67/LFO-NS nanocomposite have superior performances than pure LFO-NP and ZIF-67. The integration of ZIF-67 has enhanced the charge separation and promote the surface area of LFO-NSwhich was confirmed by various characterization techniques including TEM, HRTEM, DRS, EDX, XRD, FS, XPS, FT-IR, BET, PL, and RAMAN. The 5ZIF-67/LFO-NS sample showed significant activities for CO2 conversion, malachite green degradation, and antibiotics (cefazolin, oxacillin, and vancomycin) degradation. Furthermore, stability tests have confirmed that our optimal sample very active and stable. Furthermore, based on scavenger experiments and the photocatalytic degradation pathways, it has been established that H+ and •O2− are vital in the decomposition of MG and antibiotics. Our research work will open new gateways to prepare MOFs-Perovskites nanocatalysts for exceptional CO2 conversion, organic pollutants and antibiotics degradation.

With the use of facile single-step calcination of Zinc glutamate MOF and melamine, highly efficient ZnO/g-C3N4 nanocomposite was prepared and utilized in photocatalytic degradation of Rhodamine B (RhB), an organic pollutant. The composite's morphology, crystallinity, optical properties, and composition were determined using several analytical techniques, which include scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD), diffuse reflectance spectroscopy. The degradation of RhB over the optimized 1.0%ZnO/g-C3N4 composite is ∼1.77 fold higher compared to the pure g-C3N4 under identical conditions. The synergistic interfacial interaction between g-C3N4 and MOF derived ZnO remarkably improved the electron-hole pairs separation, which led to the exceptionally high photocatalytic activity of the composite photocatalysts. Based on the radical scavenger tests and ESR analysis, it is confirmed that •O2− as the dominant active specie facilitated the degradation of RhB over the as-prepared ZnO/g-C3N4 composites. This work will open up new insights for further research on g-C3N4 based composite materials.

Molybdenum trioxide (MoO3) is an attractive semiconductor. Thus, bandgap engineering toward photoelectronic applications is appealing yet not well studied. Here, we report the incorporation of sulfur atoms into MoO3, using sulfur powder as a source of sulfur, via a self-developed hydrothermal synthesis approach. The formation of Mo-S bonds in the MoO3 material with the synergistic effect of sulfur doping and oxygen vacancies (designated as S-MoO3−x) is confirmed using Fourier-transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR). The bandgap is tuned from 2.68 eV to 2.57 eV upon sulfur doping, as confirmed by UV-VIS DRS spectra. Some MoS2 phase is identified with sulfur doping by referring to the photoluminescence (PL) spectra and electrochemical impedance spectroscopy (EIS), allowing significantly improved charge carrier separation and electron transfer efficiency. Therefore, the as-prepared S-MoO3−x delivers a sensitive photocurrent response and splendid cycling stability. This study on the synergistic effect of sulfur doping and oxygen vacancies provides key insights into the impact of doping strategies on MoO3 performance, paving new pathways for its optimization and development in relevant fields.

Nanomaterials (NMs) have garnered significant attention in recent decades due to their versatile applications in a wide range of fields. Thanks to their tiny size, enhanced surface modifications, impressive volume-to-surface area ratio, magnetic properties, and customized optical dispersion. NMs experienced an incredible upsurge in biomedical applications including diagnostics, therapeutics, and drug delivery. This minireview will focus on notable examples of NMs that tackle important issues, demonstrating various aspects such as their design, synthesis, morphology, classification, and use in cutting-edge applications. Furthermore, we have classified and outlined the distinctive characteristics of the advanced NMs as nanoscale particles and hybrid NMs. Meanwhile, we emphasize the incredible potential of metal-organic frameworks (MOFs), a highly versatile group of NMs. These MOFs have gained recognition as promising candidates for a wide range of bio-applications, including bioimaging, biosensing, antiviral therapy, anticancer therapy, nanomedicines, theranostics, immunotherapy, photodynamic therapy, photothermal therapy, gene therapy, and drug delivery. Although advanced NMs have shown great potential in the biomedical field, their use in clinical applications is still limited by issues such as stability, cytotoxicity, biocompatibility, and health concerns. This review article provides a thorough analysis offering valuable insights for researchers investigating to explore new design, development, and expansion opportunities. Remarkably, we ponder the prospects of NMs and nanocomposites in conjunction with current technology.

It is highly desirable and of utmost importance to find eco-friendly and green approaches for a sustainable environment. Nowadays researchers from different communities have determined that it is economical and highly demanding to synthesize green nanomaterials by utilizing plants, fruits, yeast, algae, fungi, and other green techniques as stabilizers and mediators. Compared to the chemical synthesis techniques, the plant-mediated approach is considered an eco-friendly, efficient, easy, stable, and cost-effective means for the synthesis of nanomaterials. Among various nano-size materials, Graphitic carbon nitride, g-C3N4, (CN) belongs to a new class of multifunctional metal-free n-type semiconductors. It has a polymeric structure with many potential applications in agriculture and energy sectors and other fields. So, it is highly demanding to explore the green synthesis approaches and their utilization for nanomaterials, especially g-C3N4. In this review, we comprehensively explored the green g-C3N4 based nanomaterials, their preparation, properties, applications, and opportunities. Adding more, this study aims to explore all feasible green synthesis approaches, applications, characterization techniques, and modification methods. Apart from this, the current statutes and future prospectus of the green g-C3N4 based nanomaterials are also explored. Finally, this work will open a new gateway for the synthesis of green g-C3N4 based nanomaterials and their utilization for a sustainable environment.

Abstract Water constitutes ≈70–90% of the organism's body by mass and is highly important for its survival. Water contains a variety of chemical contaminants introduced by various sectors, resulting in contamination that has a direct impact on the ecosystem. Various approaches are in practice to tackle these issues. Among these, semiconductor photocatalysis appears to be the cutting‐edge technology for the degradation of wastewater contaminants. Herein, the fabrication of Fe3O4−SiO2 nanocomposite via facile co‐precipitation and Stober methods are reported. Various characterization techniques are employed for the structural elucidation, morphology, crystallinity, and stability of the as‐prepared composite. The nanocomposite is employed in catalytic and photocatalytic applications toward the removal of methylene blue (MB) and methyl orange (MO) dyes from a comparative perspective. It is observed that the composite can remove about 93% of MB and 51% of MO within 7 and 6 h, respectively. These findings indicate that the nanocomposite has a higher MB removal effectiveness than the MO. This trend can be accredited to the difference in the chemical structure of both dyes. The nanocomposite is also evaluated for antioxidant and antileishmanial activity, and it is shown to be quite effective even at very low concentrations.

Water contamination is a ubiquitous issue for all countries and territories worldwide. Among others, pesticides, drugs, heavy metals, and phosphates play a special role in terms of pollutants due to their toxicity and large-scale applications in industrial and agricultural activities. In order to provide cleaner freshwater for the world’s population, two types of actions are required: preventing/limiting the pollution that might occur during our daily activities and decontaminating the already exposed/contaminated water sources. One of the key points in the decontamination process is to create as few as possible side effects with the solutions applied. For this reason, in the case of the mentioned types of pollutants but not limited only to them, the use of environmentally friendly materials is more than welcome. Biochar qualifies as one of these materials, and its field of applications expands to larger scientific and industrial areas every day. Moreover, it can be functionalized in order to improve its properties in terms of pollutant removal efficiency. This paper summarizes the most recent developments in the field of water decontamination using biochar or biochar-based materials in order to remove pesticides, drugs, heavy metals, and phosphates from contaminated aqueous environments. Also, the removal of phosphorus from wastewater using biochar is considered. This removal can be a key controlling factor for the wastewater, which is obtained as a residual of agricultural activities. Indeed, due to the excessive use of chemical fertilizers, eutrophication in such kinds of wastewater can be a serious challenge.

Introduction: The genus Euphorbia is known to contain diterpenoids, and several isolated compounds which exhibited biological activities including significant multidrug resistance reversal effects. This work is focused on the isolation, in vitro and in silico studies of two natural bio-active flavonoids (1 & 2) isolated from Euphorbia pulcherrima bark for the very first time. Methods: The phytochemical investigation resulted in the identification of two flavonoids: 3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-4H-chromen-4-one (1) and 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-methoxy-4H-chromen-4-one (2), which were isolated for the first time from Euphorbia pulcherrima. Results: The chemical structures of the two isolated compounds were confirmed by 1H NMR, 13C NMR, and ESI-HRMS spectral data. The Bioactivity activity of these compounds was evaluated; results revealed that compounds 1 & 2 exhibit promising urease inhibitory potential with IC50 values of 15.3 ± 2.13 μM and 19.0 ± 2.43 μM, respectively, whereas the positive control thiourea had an IC50 of 21.0 ± 0.23 μM. Similarly, these compounds were also evaluated against the tyrosinase enzyme; results showed that compound 1 displays significant inhibitory activity with an IC50 value of 48.7 ± 2.19 μM, whereas compound 2 exhibited a moderate effect with an IC50 value of 74.8 ± 1.79 μM, when compared with the standard (alpha-kojic acid, IC50 = 47.6 ± 0.67 μM). Additionally, compounds 1 and 2 also exhibited anti-glycation and phosphodiesterase inhibitory activities. Conclusion: Studies dealing with the drug like properties such as in silico screening (docking study) was also carried out to discover the structural features of both compounds 1 and 2. Results indicated that the docking scores of compounds 1 and 2 are in agreement with their IC50 values. Key messages Isolation and characterization of two bioactive flavonoids (1 and 2) from Euphorbia pulcherrima. In silico and in vitro enzyme inhibition studies were conducted to identify the therapeutic potential of flavonoids 1 and 2. Drug-like properties were calculated to discover important pharmacophoric features.

The use of pheromone traps can minimize the excess application of synthetic insecticides, while can also benefit the environment. The use of pheromone traps has been promoted and suggested to vegetable farmers of Bangladesh for widespread adoption. However, the majority of farmers have continued to spray insecticides instead of using pheromone traps. The present study investigated the factors influencing farmers' adoption, dis-adoption, and non-adoption behavior of pheromone traps for managing insect pests. Primary data were collected from 438 vegetable growers. Data were analyzed using descriptive statistics and multinomial logistic regression. About 27% of the farmers abandoned the technique shortly after it was adopted as it was time-consuming to manage insect pests. Marginal effect analysis revealed that the likelihood of continued adoption was 34.6% higher for farmers who perceived that pheromone traps were useful in controlling insect pests. In contrast, the likelihood of dis-adoption was 16.5% and 10.4% higher for farmers who maintained communication with private pesticide company agents and neighbor farmers, respectively. Extension services by government extension personnel might be encouraged and maintained as a key component in increasing farmer awareness regarding the use of pheromone trap. Strategies to promote pheromone traps in vegetable production should highlight the positive impacts to farmers and the environment, as this would most likely lead to their continued and widespread use after initial adoption.

Abstract The photocatalytic performance of g-C3N4 for CO2 conversion is still inadequate by several shortfalls including the instability, insufficient solar light absorption and rapid charge carrier’s recombination rate. To solve these problems, herein, noble metals (Pt and Au) decorated Sr-incorporated g-C3N4 photocatalysts are fabricated via the simple calcination and photo-deposition methods. The Sr-incorporation remarkably reduced the g-C3N4 band gap from 2.7 to 2.54 eV, as evidenced by the UV–visible absorption spectra and the density functional theory results. The CO2 conversion performance of the catalysts was evaluated under visible light irradiation. The Pt/0.15Sr-CN sample produced 48.55 and 74.54 µmol h−1 g−1 of CH4 and CO, respectively. These amounts are far greater than that produced by the Au/0.15Sr-CN, 0.15Sr-CN, and CN samples. A high quantum efficiency of 2.92% is predicted for the Pt/0.15Sr-CN sample. Further, the stability of the photocatalyst is confirmed via the photocatalytic recyclable test. The improved CO2 conversion performance of the catalyst is accredited to the promoted light absorption and remarkably enhanced charge separation via the Sr-incorporated mid gap states and the localized surface plasmon resonance effect induced by noble metal nanoparticles. This work will provide a new approach for promoting the catalytic efficiency of g-C3N4 for efficient solar fuel production.

This work reports synthesis of an efficient MoO3/ZnCo2O4@CeO2, bifunctional heterogeneous catalyst for profitable conversion of corncob biomass into Levulinic acid. The physiochemical properties of the catalyst were studied by TG-DTA, BET, XRD, FESEM/SEM, EDX-Mapping and TPD to correlate them with the catalytic activity. The results exposed that the synthesized catalyst showed improved catalytic performance, providing Levulinic acid yield of 70.1% under 8 wt% catalyst loading at 200 °C temperature for 220 min. Moreover, the catalyst presented sufficient reusability and recycled for at least 3 times for Levulinic acid production from the biomass without any loss in the catalytic activity.

This research work focuses on the isolation and thermo-chemical modification of cellulose and its application as an adsorbent for the removal of organic pollutants. The used cellulose was collected from a locally available plant (Olive Europa) commonly called Zaitoon. The stem branches of Zaitoon were collected and then kept in water for 40–45 days at room temperature to extract the cellulose fibers. These cellulose fibers were then kept in the Soxhlet apparatus for washing in n-hexane for 72 h. The purified cellulose was divided into three parts: one part was subjected to thermal activation (TAC), the second was modified chemically (CMC) with Benzyl Chloride, while the last one remained un-functionalized (UFC). All the three forms of cellulose were characterized via FTIR and SEM, then utilized for the removal of Titan Yellow (TY) dye from aqueous media via adsorption process by varying the contact time, temperature, concentration of dye and type, and dose of adsorbent. The adsorption efficiencies of all adsorbents were compared under different experimental variables. Thermally activated cellulose showed the best results for the removal of TY compared with other materials. The calculated removal percentage of TY was found to be 97.69, 94.83, 94.83, and 98% under equilibrium conditions of contact time, temperature, adsorbent dose, and TY concentration. Similarly, the uptake capacities of TAC under optimal experimental conditions were found to be 19.56, 18.96, 18.52, and 18.75 mg/g. Thermodynamic studies of TAC, CMC, and UFC showed that the values of ΔG are negative, while those of ΔH and ΔS are positive in all cases and at all temperatures. This indicates that the TY elimination process is endothermic and spontaneous with an entropy-driven nature. The obtained results indicate that the as-fabricated low-cost biomaterials can effectively remove dyes from wastewater through physicochemical interactions. The removal process was influenced by the nature of the adsorbent and the operating variables.

The watershed area of the Mangla Reservoir spans across the Himalayan region of India and Pakistan, primarily consisting of the Jhelum River basin. The area is rugged with highly elevated, hilly terrain and relatively thin vegetation cover, which significantly increases the river’s sediment output, especially during the monsoon season, leading to a decline in the reservoir’s storage capacity. This work assesses the soil erosion risk in the Jhelum River watershed (Azad Jammu and Kashmir (AJ&K), Pakistan) using the Revised Universal Soil Loss Equation of (RUSLE). The RUSLE components, including the conservation support or erosion control practice factor (P), soil erodibility factor (K), slope length and slope steepness factor (LS), rainfall erosivity factor (R), and crop cover factor (C), were integrated to compute soil erosion. Soil erosion risk and intensity maps were generated by computing the RUSLE parameters, which were then integrated with physical factors such as terrain units, elevation, slope, and land uses/cover to examine how these factors affect the spatial patterns of soil erosion loss. The 2021 rainfall data were utilized to compute the rainfall erosivity factor (R), and the soil erodibility (K) map was created using the world surface soil map prepared by the Food and Agriculture Organization (FAO). The slope length and slope steepness factor (LS) were generated in the highly rough terrain using Shuttle Radar Topography Mission Digital Elevation Model (SRTM DEM). The analysis revealed that the primary land use in the watershed was cultivated land, accounting for 27% of the area, and slopes of 30% or higher were present across two-thirds of the watershed. By multiplying the five variables, the study determined that the annual average soil loss was 23.47 t ha−1 yr−1. In areas with dense mixed forest cover, soil erosion rates ranged from 0.23 t ha−1 yr−1 to 25 t ha−1 yr−1. The findings indicated that 55.18% of the research area has a low erosion risk, 18.62% has a medium erosion risk, 13.66% has a high risk, and 11.6% has a very high erosion risk. The study’s findings will provide guidelines to policy/decision makers for better management of the Mangla watershed.

A common challenge forward-looking utilities are facing when deploying advanced applications that facilitate voltage optimization and service restoration is to provide adequate sensor data for a Distribution System State Estimator (DSSE) so that it provides sufficiently accurate estimates of the system states to enable these applications in an operational environment. We developed a stochastic method that informs telemetry and operational forecasting requirements by quantifying the DSSE performance in supporting advanced applications. The performance metric used is the α risk, which is the likelihood of a DSSE giving a false positive when determining if voltage and loading constraints are met. We applied this method to six real-world industrial/commercial/residential distribution circuits and evaluated α risk improvements provided by circuit-level sensors and operational forecasting. The results show that a combination of sensor deployment schemes was needed to reduce the α risk for undervoltage to effectively zero. Also, sensors deployed at large loads significantly reduce c risks on industrial/commercial circuits while operational forecasting consistently reduces α risks on all circuits. The practical method does not require advanced mathematics and can be readily used by utilities to inform grid modernization investments in sensor technologies so that advanced applications can be executed optimally and violation-free.

Electrocatalytic urea oxidation reaction (UOR) is regarded as an effective yet challenging approach for the degradation of urea in wastewater into harmless N2 and CO2. To overcome the sluggish kinetics, catalytically active sites should be rationally designed to maneuver the multiple key steps of intermediate adsorption and desorption. Herein, we demonstrate that metal-organic frameworks (MOFs) can provide an ideal platform for tailoring binary active sites to facilitate the rate-determining steps, achieving remarkable electrocatalytic activity toward UOR. Specifically, the MOF (namely, NiMn0.14-BDC) based on Ni/Mn sites and terephthalic acid (BDC) ligands exhibits a low voltage of 1.317 V to deliver a current density of 10 mA cm-2. As a result, a high turnover frequency (TOF) of 0.15 s-1 is achieved at a voltage of 1.4 V, which enables a urea degradation rate of 81.87% in 0.33 M urea solution. The combination of experimental characterization with theoretical calculation reveals that the Ni and Mn sites play synergistic roles in maneuvering the evolution of urea molecules and key reaction intermediates during the UOR, while the binary Ni/Mn sites in MOF offer the tunability for electronic structure and d-band center impacting on the intermediate evolution. This work provides important insights into active site design by leveraging MOF platform and represents a solid step toward highly efficient UOR with MOF-based electrocatalysts.

Abstract A typical Z-scheme system is composed of two photocatalysts which generate two sets of charge carriers and split water into H2 and O2 at different locations. Scientists are struggling to enhance the efficiencies of these systems by maximizing their light absorption, engineering more stable redox couples, and discovering new O2 and H2 evolutions co-catalysts. In this work, Au decorated WO3/g-C3N4 Z-scheme nanocomposites are fabricated via wet-chemical and photo-deposition methods. The nanocomposites are utilized in photocatalysis for H2 production and 2,4-dichlorophenol (2,4-DCP) degradation. It is investigated that the optimized 4Au/6% WO3/CN nanocomposite is highly efficient for production of 69.9 and 307.3 µmol h−1 g−1 H2 gas, respectively, under visible-light (λ > 420 nm) and UV–visible illumination. Further, the fabricated 4Au/6% WO3/CN nanocomposite is significant (i.e., 100% degradation in 2 h) for 2,4-DCP degradation under visible light and highly stable in photocatalysis. A significant 4.17% quantum efficiency is recorded for H2 production at wavelength 420 nm. This enhanced performance is attributed to the improved charge separation and the surface plasmon resonance effect of Au nanoparticles. Solid-state density functional theory simulations are performed to countercheck and validate our experimental data. Positive surface formation energy, high charge transfer, and strong non-bonding interaction via electrostatic forces confirm the stability of 4Au/6% WO3/CN interface.

Organic dyes with enduring colors which are malodorous are a significant source of environmental deterioration due to their virulent effects on aquatic life and lethal carcinogenic effects on living organisms. In this study, the adsorption of methyl green (MG), a cationic dye, was achieved by using ZIF-67, which has been deemed an effective adsorbent for the removal of contaminants from wastewater. The characterization of ZIF-67 was done by FTIR, XRD, and SEM analysis. The adsorption mechanism and characteristics were investigated with the help of control batch experiments and theoretical studies. The systematical kinetic studies and isotherms were sanctioned with a pseudo-second-order model and a Langmuir model (R2 = 0.9951), confirming the chemisorption and monolayer interaction process, respectively. The maximum removal capacities of ZIF-67 for MG was 96% at pH = 11 and T = 25 °C. DFT calculations were done to predict the active sites in MG by molecular electrostatic potential (MEP). Furthermore, both Molecular dynamics and Monte Carlo simulations were also used to study the adsorption mechanism.

The China-Pakistan Economic Corridor (CPEC) is a flagship project under the Belt and Road Initiative (BRI); and its launch in 2015 was regarded as a landmark event in the history of the Sino-Pakistani relationship. With a budget amounting to over $62 billion, it has become the foremost regional integration initiative between China and Pakistan. The project is also open to all interested regional stakeholders, among which Central Asia is one of the most important in geopolitical terms. Located in a landlocked but resource-rich region, Central Asian countries need better access to regional markets including Pakistan, China, India, and the countries of West Asia. Pakistan and China have huge energy demands that can be satisfied by growing trade with Central Asia. Thus, the CPEC will not only benefit Pakistan and China, but it also presents a strategic opportunity for Turkmenistan, Uzbekistan, Kyrgyzstan, Kazakhstan, and Tajikistan to transport their goods more easily and gain competitiveness in regional and global markets.

Due to their unique layered microstructure, the presence of various functional groups at the surface, earth abundance, and attractive electrical, optical, and thermal properties, MXenes are considered promising candidates for the solution of energy- and environmental-related problems. It is seen that the energy conversion and storage capacity of MXenes can be enhanced by changing the material dimensions, chemical composition, structure, and surface chemistry. Hence, it is also essential to understand how one can easily improve the structure–property relationship from an applied point of view. In the current review, we reviewed the fabrication, properties, and potential applications of MXenes. In addition, various properties of MXenes such as structural, optical, electrical, thermal, chemical, and mechanical have been discussed. Furthermore, the potential applications of MXenes in the areas of photocatalysis, electrocatalysis, nitrogen fixation, gas sensing, cancer therapy, and supercapacitors have also been outlooked. Based on the reported works, it could easily be observed that the properties and applications of MXenes can be further enhanced by applying various modification and functionalization approaches. This review also emphasizes the recent developments and future perspectives of MXenes-based composite materials, which will greatly help scientists working in the fields of academia and material science.

Wastewater from the textile industries contaminates the natural water and affects the aquatic environment, soil fertility and biological ecosystem through discharge of different hazardous effluents. Therefore, it is essential to remove such dissolved toxic materials from water by applying more efficient techniques. We performed a comparative study on the removal of rhodamine B (RhB) and Nile blue (NB) from water through a catalytic/photocatalytic approach while using a CuO–SiO2 based nanocomposite. The CuO–SiO2 nanocomposite was synthesized through a sol–gel process using copper nitrate dihydrate and tetraethylorthosilicate as CuO and SiO2 precursors, respectively, with ammonia solution as the precipitating agent. The synthesized nanocomposites were characterized, for their structure, morphology, crystallinity, stability, surface area, pore size and pore volume, by using a scanning electron microscope (SEM), transmission electron microscope (TEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Brunauer–Emmett–Teller (BET) techniques. The CuO–SiO2 nanocomposite was used for potential environmental applications in the terms of its catalytic and photocatalytic activities toward the degradation of rhodamine B (RhB) and Nile blue (NB) dyes, in the presence and absence of light, while monitoring the degradation process of dyes by UV-Visible spectroscopy. The catalytic efficiency of the same composite was studied and discussed in terms of changes in the chemical structures of dyes and other experimental conditions, such as the presence and absence of light. Moreover, the composite showed 85% and 90% efficiency towards the removal of rhodamine B and Nile blue dyes respectively. Thus, the CuO–SiO2 nanocomposite showed better efficiency toward removal of Nile blue as compared to rhodamine B dye while keeping other experimental variables constant. This can be attributed to the structure–property relationships and compatibility of a catalyst with the molecular structures of dyes.

This work reports the formation of a novel adsorbent, prepared by activating bentonite with cinnamic acid, which is highly efficient to remove dyes from wastewater. The adsorption efficiency of the cinnamic acid activated bentonite was compared with unmodified bentonite by removing methyl orange and rhodamine-B from polluted water. The characterization was performed through X-ray diffraction (XRD) Fourier transform infrared (FTIR) and scanning electron microscopy (SEM). The results indicated that acidic pH and low temperature were more suitable for the selected dyes adsorption. The analysis of the data was done by the Langmuir and Freundlich isotherms; the Freundlich isotherm showed more suitability for the equilibrium data. The data were further analyzed by pseudo-first and pseudo-second-order models to study adsorption kinetics. The results showed that methyl orange and rhodamine-B adsorption obeyed pseudo-order kinetics. The results obtained from this research suggested that acid activation of bentonite with cinnamic acid increased the surface area of the clay and hence enhanced its adsorption efficiency. The maximum adsorption efficiency for the removal of methyl orange and rhodamine-B was up to 99.3 mg g−1 and 44.7 mg g−1, respectively, at 25 °C. This research provides an economical modification technique of bentonite, which makes it cost-effective and a good adsorbent for wastewater treatment.

It is highly desired to enhance charge separation and O2 adsorption of the pyropheophorbide-a (Ppa) to promote visible-light activity and stability. Herein, Ppa modified 001-facet-exposed TiO2 nanosheets (Ppa/001T) nanocomposites with different weight ratios were fabricated via the self-assembly approach by OH induced. Compared with the bare Ppa, the 8% amount optimized 8Ppa/001T sample displayed 41-fold enhanced activity for degradation of Ametryn (AME) under visible-light irradiation. The promoted photoactivities could be attributed to the accelerated charge carrier’s separation by coupling TiO2 as thermodynamic platform for accepting the photoelectrons with high energy from Ppa and the promoted O2 adsorption because of the residual fluoride on TiO2. As for this, a distinctive two radicals (•O2− and •OH) involved pathway of AME degradation is carried out, which is different from the radical pathway dominated by •O2− for the bare Ppa. This work is of utmost importance since it gives us detailed information regarding the charge carrier’s separation and the impact of the radical pathway that will pave a new approach toward the design of high activity visible-light driven photocatalysts.

The 2021–2022 flood is one of the most serious flood events in Malaysian history, with approximately 70,000 victims evacuated daily, 54 killed and total losses up to MYR 6.1 billion. From this devastating event, we realized the lack of extreme precipitation and flood inundation information, which is a common problem in tropical regions. Therefore, we developed a Rapid Extreme TRopicAl preCipitation and flood inundation mapping framEwork (RETRACE) by utilizing: (1) a cloud computing platform, the Google Earth Engine (GEE); (2) open-source satellite images from missions such as Global Precipitation Measurement (GPM), Sentinel-1 SAR and Sentinel-2 optical satellites; and (3) flood victim information. The framework was demonstrated with the 2021–2022 Malaysia flood. The preliminary results were satisfactory with an optimal threshold of five for flood inundation mapping using the Sentinel-1 SAR data, as the accuracy of inundated floods was up to 70%. Extreme daily precipitation of up to 230 mm/day was observed and resulted in an inundated area of 77.43 km2 in Peninsular Malaysia. This framework can act as a useful tool for local authorities and scientists to retrace the extreme precipitation and flood information in a relatively short period for flood management and mitigation strategy development.

This paper proposes an AC micro-grid structure, which was based on diesel engine, synchronous generator and hybrid energy storage (HES) subsystem, consisting of battery and ultra-capacitor. In system operation, the diesel generator works as the sole voltage source of the micro-grid under islanding mode and the HES cooperate to achieve the power balance of the system. The corresponding energy management strategy was proposed, where the net power of the micro-grid is separated into high and low frequency components. The high frequency part is suppressed by the ultra-capacitor unit, whereas the low frequency part is compensated by the diesel generator and the battery unit together. Through the designed energy management strategy, power balanced of the micro-grid system can be achieved. MATLAB/SIMULINK simulation results under different conditions have verified this proposed micro-grid structure and the proposed energy management strategy. Keywords: AC micro-grid, Diesel generator, Power balance, Ultra-capacitor and battery

Objective: To explore the in vitro pharmacological activities of fruit of Diospyros malabarica. Method: 70% ethanolic extracts of Diospyros malabarica was screened against ten pathogenic bacteria, five strains of gram +ve, five strains of gram –ve bacteria and fungi by using disc diffusion method. Moreover, to study the toxicity of this fruit, we conducted a saltwater shrimp lethality bioassay based on the ability to kill laboratory cultured brine shrimps (Artemiasalina). Results: Fruits extracts were found to exhibit antimicrobial activity against bacterial pathogens with the zone of inhibition ranges between 13mm to 19mm. Fruit Extracts was also tested for its antifungal activity against fungal strains exhibiting zone of inhibition ranges from 14 mm to 19 mm. The fruit extract of Diospyros malabarica shows significant lethality towards brine shrimps at LD50 value of 93.55 ppm. Conclusion: Plant extracts is potentially effective in suppressing microbial and fungal growth. As fruit extracts has significant LD50 value thus it can be further used for cancer cell line studies.

Supercapacitors (SCs) have received much interest due to their enhanced electrochemical performance, superior cycling life, excellent specific power, and fast charging–discharging rate. The energy density of SCs is comparable to batteries; however, their power density and cyclability are higher by several orders of magnitude relative to batteries, making them a flexible and compromising energy storage alternative, provided a proper design and efficient materials are used. This review emphasizes various types of SCs, such as electrochemical double-layer capacitors, hybrid supercapacitors, and pseudo-supercapacitors. Furthermore, various synthesis strategies, including sol-gel, electro-polymerization, hydrothermal, co-precipitation, chemical vapor deposition, direct coating, vacuum filtration, de-alloying, microwave auxiliary, in situ polymerization, electro-spinning, silar, carbonization, dipping, and drying methods, are discussed. Furthermore, various functionalizations of SC electrode materials are summarized. In addition to their potential applications, brief insights into the recent advances and associated problems are provided, along with conclusions. This review is a noteworthy addition because of its simplicity and conciseness with regard to SCs, which can be helpful for researchers who are not directly involved in electrochemical energy storage.

Electrochemical CO2 reduction reaction (CO2RR) provides a promising approach to curbing harmful emissions contributing to global warming. However, several challenges hinder the commercialization of this technology, including high overpotentials, electrode instability, and low Faradic efficiencies of desirable products. Several materials have been developed to overcome these challenges. This mini-review discusses the recent performance of various cobalt (Co) electrocatalysts, including Co-single atom, Co-multi metals, Co-complexes, Co-based metal–organic frameworks (MOFs), Co-based covalent organic frameworks (COFs), Co-nitrides, and Co-oxides. These materials are reviewed with respect to their stability of facilitating CO2 conversion to valuable products, and a summary of the current literature is highlighted, along with future perspectives for the development of efficient CO2RR.

Covalent organic frameworks (COFs) are emerging crystalline polymeric materials with highly ordered intrinsic and uniform pores. Their synthesis involves reticular chemistry, which offers the freedom of choosing building precursors from a large bank with distinct geometries and functionalities. The pore sizes of COFs, as well as their geometry and functionalities, can be pre-designed, giving them an immense opportunity in various fields. In this mini-review, we will focus on the use of COFs in the removal of environmentally hazardous metal ions and chemicals through adsorption and separation. The review will introduce basic aspects of COFs and their advantages over other purification materials. Various fabrication strategies of COFs will be introduced in relation to the separation field. Finally, the challenges of COFs and their future perspectives in this field will be briefly outlined.

Photocatalysis is a classical solution to energy conversion and environmental pollution control problems. In photocatalysis, the development and exploration of new visible light catalysts and their synthesis and modification strategies are crucial. It is also essential to understand the mechanism of these reactions in the various reaction media. Recently, bismuth and graphene’s unique geometrical and electronic properties have attracted considerable attention in photocatalysis. This review summarizes bismuth-graphene nanohybrids’ synthetic processes with various design considerations, fundamental mechanisms of action, heterogeneous photocatalysis, benefits, and challenges. Some key applications in energy conversion and environmental pollution control are discussed, such as CO2 reduction, water splitting, pollutant degradation, disinfection, and organic transformations. The detailed perspective of bismuth-graphene nanohybrids’ applications in various research fields presented herein should be of equal interest to academic and industrial scientists.

Polymer networks were prepared by Steglich esterification using poly(sorbitol adipate) (PSA) and poly(sorbitol adipate)-graft-poly(ethylene glycol) mono methyl ether (PSA-g-mPEG12) copolymer. Utilizing multi-hydroxyl functionalities of PSA, poly(ethylene glycol) (PEG) was first grafted onto a PSA backbone. Then the cross-linking of PSA or PSA-g-mPEG12 was carried out with disuccinyl PEG of different molar masses (Suc-PEGn-Suc). Polymers were characterized through nuclear magnetic resonance (NMR) spectroscopy, gel permeation chromatography (GPC), and differential scanning calorimetry (DSC). The degree of swelling of networks was investigated through water (D2O) uptake studies, while for detailed examination of their structural dynamics, networks were studied using 13C magic angle spinning NMR (13C MAS NMR) spectroscopy, 1H double quantum NMR (1H DQ NMR) spectroscopy, and 1H pulsed field gradient NMR (1H PFG NMR) spectroscopy. These solid state NMR results revealed that the networks were composed of a two component structure, having different dipolar coupling constants. The diffusion of solvent molecules depended on the degree of swelling that was imparted to the network by the varying chain length of the PEG based cross-linking agent.

Gold nanoparticles (Au NPs) play a significant role in science and technology because of their unique size, shape, properties and broad range of potential applications. This review focuses on the various approaches employed for the synthesis, modification and functionalization of nanostructured Au. The potential catalytic applications and their enhancement upon modification of Au nanostructures have also been discussed in detail. The present analysis also offers brief summaries of the major Au nanomaterials synthetic procedures, such as hydrothermal, solvothermal, sol-gel, direct oxidation, chemical vapor deposition, sonochemical deposition, electrochemical deposition, microwave and laser pyrolysis. Among the various strategies used for improving the catalytic performance of nanostructured Au, the modification and functionalization of nanostructured Au produced better results. Therefore, various synthesis, modification and functionalization methods employed for better catalytic outcomes of nanostructured Au have been summarized in this review.

In this research work, physical, chemical, morphological, and mechanical behavior as partial replacement of fine aggregate in concrete. Stone dust was acquired from three different sources i.e. Nowshera, Dara, and Besai, while concrete was kept at a ratio of 1:2:4 and water to cement ratio at 0.5 as per ASTM standards for considerable workability. The compressive strength, ultrasonic pulse velocity (UPV), its correlation, density, durability test, x-ray fluorescence (XRF) analysis, and Scanning electron microscopy was carried out. Compressive strength at curing ages of 7, 14, and 28 days with 20%, 30%, and 40% replacement of sand was incorporated in concrete. The results indicated a slight increase in compressive strength at 20% replacement level for the Besai Concrete (BC), Nowshera Concrete (NC), and Dara Concrete (DC). For durability analysis; Rapid Chloride Permeability Test (RCPT) carried out on hardened stone dust-based concrete shows that with the addition of stone dust the voids between fine and coarse aggregates are filled up, less charge will pass, and ultimately durability is increased as per ASTM C 1202. The chemical composition of the stone dust samples, through XRF analysis, indicated that Silica dioxide (SiO2) compounds present in (NC), (DC), and (BC) were 13.34%, 12.339% & 11.593% respectively. The maximum compressive strength development in NC was possibly due to the presence of SiO _2 compound in excess quantity in Nowshera stone dust as compared to other samples tested. Hence it can be recommended that locally available stone dust in Peshawar and its surrounding are suitable for a maximum of 40% replacement level.

This study was performed to standardize the ultrasound estimated bladder weight as an additional non-invasive test for the measurement of the bladder outflow obstruction and to measure the therapeutic effects of bladder outflow obstruction in the follow-up after surgical correction of obstruction. This study was conducted from December 2012 to May 2014 where the sample size was 55 and sampling technique was purposive. In bladder outflow obstruction patient, transabdominal sonography was performed using a 7.5 MHz. probe. The anterior bladder wall thickness was measured in three points in the midline 1 cm apart and the average value was recorded. After that bladder volume was measured by ultrasonogram. In pre- and post-operative groups ultrasound estimated bladder weight was measured from bladder wall thickness and bladder volume. In this study, the mean ± SD of age was 48.8 ± 15.0 years. In bladder outflow obstruction patient, the pre-operative ultrasound estimated bladder weight was 117 ± 45.1 g which was reduced to 53.9 ± 10.8 g three months after surgical correction of obstruction. The ultrasound estimated bladder weight is a non-invasive, cheap and easily available additional diagnostic tool for detecting bladder outflow obstruction as well as it can measure the therapeutic effects in post-operative period.

Photocatalytic removal of organic pollution such as waste colored dyes was a promising technique for environment technique. However, effective photocatalysts were needed to enhance the photocatalytic efficiency. Ag/AgCl was regarded as high performance catalyst for photocatalytic degradation. Ag/AgCl nanoparticles were biochemically prepared with metabolin of living fungi which was used as reductant and characterized by X-Ray diffraction (XRD), UV-visible spectroscopy and transmission electron microscopy (TEM). The Ag/AgCl nanoparticle composites showed spherical aggregation shape with an average size of about 3–5 nm which is well inside the quantum regime. The UV-visible study showed that Ag/AgCl nanoparticles had strong visible light absorption and exhibited excellent visible-light-driven photocatalytic performance. Photocatalytic results indicated that the obtained Ag/AgCl nanoparticles were suitable for photocatalytic removal of RhB dye under visible light irradiation. The excellent photocatalytic activities could be attributed to the quantum size nanoparticles and the Plasmon resonance of Ag/AgCl composites.