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The problem that this study addresses is to understand how microwave radiation is able to degrade genomic DNA of E. coli. In addition, a comparative study was made to evaluate the suitability of a high-throughput automated electrophoresis platform for quantifying the DNA degradation under microwave radiation. Overall, this study investigated the genomic DNA degradation of E. coli under microwave radiation using automated gel electrophoresis. To examine the viable organisms and degradation of genomic DNA under microwave exposure, we used three methods: (1) post-microwave exposure, where E. coli was enumerated using modified mTEC agar method using membrane filtration technique; (2) extracted genomic DNA of microwaved sample was quantified using the Qubit method; and (3) automated gel electrophoresis, the TapeStation 4200, was used to examine the bands of extracted DNA of microwaved samples. In addition, to examine the impacts of microwaves, E. coli colonies were isolated from a fecal sample (dairy cow manure), these colonies were grown overnight to prepare fresh E. coli culture, and this culture was exposed to microwave radiation for three durations: (1) 2 min; (2) 5 min; and (3) 8 min. In general, Qubit values (ng/µL) were proportional to the results of automated gel electrophoresis, TapeStation 4200, DNA integrity numbers (DINs). Samples from exposure studies (2 min, 5 min, and 8 min) showed no viable E. coli. Initial E. coli levels (at 0 min microwave exposure) were 5 × 108 CFU/mL, and the E. coli level was reduced to a non-detectable level within 2 min of microwave exposure. The relationships between Qubit and TapeStation measurements was linear, except for when the DNA level was lower than 2 ng/µL. In 8 min of microwave exposure, E. coli DNA integrity was reduced by 61.7%, and DNA concentration was reduced by 81.6%. The overall conclusion of this study is that microwave radiation had a significant impact on the genomic DNA of E. coli, and prolonged exposure of E. coli to microwaves can thus lead to a loss of genomic DNA integrity and DNA concentrations.

Drier and hotter conditions linked with anthropogenic climate change can increase wildfire frequency and severity, influencing terrestrial and aquatic carbon cycles at broad spatial and temporal scales. The impacts of wildfire are complex and dependent on several factors that may increase terrestrial deposition and the influx of dissolved organic matter (DOM) from plants into nearby aquatic systems, resulting in the darkening of water color. We tested the effects of plant biomass quantity and its interaction with fire (burned vs. unburned plant biomass) on dissolved organic carbon (DOC) concentration and degradation (biological vs. photochemical) and DOM composition in 400 L freshwater ponds using a gradient experimental design. DOC concentration increased nonlinearly with plant biomass loading in both treatments, with overall higher concentrations (>56 mg/L) in the unburned treatment shortly after plant addition. We also observed nonlinear trends in fluorescence and UV-visible absorbance spectroscopic indices as a function of fire treatment and plant biomass, such as greater humification and specific UV absorbance at 254 nm (a proxy for aromatic DOM) over time. DOM humification occurred gradually over time with less humification in the burned treatment compared to the unburned treatment. Both burned and unburned biomass released noncolored, low molecular weight carbon compounds that were rapidly consumed by microbes. DOC decomposition exhibited a unimodal relationship with plant biomass, with microbes contributing more to DOC loss than photodegradation at intermediate biomass levels (100-300 g). Our findings demonstrate that the quantity of plant biomass leads to nonlinear responses in the dynamics and composition of DOM in experimental ponds that are altered by fire, indicating how disturbances interactively affect DOM processing and its role in aquatic environments.

We investigate the degradation mechanisms of In0.2Ga0.8N/GaN light emitting diodes through combined experimental analysis and simulations. The devices were submitted to constant current stress at 100 mA. Depending on the measuring current level, two degradation trends were observed: at high test currents (e.g. 200 mA), a monotonic decrease in optical power was observed; at low test currents (e.g. 5 mA), an initial degradation was observed, followed by an improvement in device efficiency (positive ageing). For the first time, such recovery effect was analyzed and modeled, as due to the generation of charged defects at the InGaN/GaN interface, resulting in the increase in the injection efficiency at low bias levels. The role of interface defects was validated by means of numerical simulations, with good agreement with the experimental data. [ABSTRACT FROM AUTHOR]

This study investigated the degradation mechanisms of SiC-MgAl 2 O 4 refractory materials in a bench-scale entrained flow gasifier. Layered degradation and protective SiO 2 formation on SiC aggregates were observed by macroscopic, microscopic, phase analysis, and thermodynamic calculations. A comparative investigation of erosion rates revealed that SiC-MgAl 2 O 4 materials located away from the burner had an unusually low erosion rate of 0.0017 mm/h, which was significantly lower than that reported in their counterparts situated near the burner (0.0167 mm/h). This performance surpassed even that of high-chrome refractory materials positioned at a similar distance from the burner. The findings underscore the remarkable durability of SiC-MgAl 2 O 4 , demonstrating its significant potential as a sustainable and chrome-free alternative for application in harsh gasification conditions. The environment-specific degradation patterns, characterized by the formation of mullite and cordierite, revealed the complex interaction between refractory materials and gasification environments. This understanding offers valuable insights that can inform the development and implementation of chrome-free refractory materials under industrial gasification conditions. [ABSTRACT FROM AUTHOR]

In this paper, summarise the characterization and synthesis of the pure and Eu:WO 3 nanoparticles and their applications in photocatalytic and antibacterial activity. The monoclinic phase confirmed by the XRD analysis of the prepared specimens. SEM and HR-TEM scrutiny revealed nanoplate morphology scrutiny. EDS and XPS scrutiny confirmed the composition of elements of Eu, O, and W. FTIR analysis likely used for additional confirmation of functional groups. UV–Vis Analysis determined the band gap energy (Eg) of the nanoparticles, which decreased with raising the concentration of Eu doping. Optical properties of the band gap energy decreased with raising the concentration of Eu doping. Photocatalytic activity of the nanoparticles exhibited high photocatalytic activity, with a 95.3 % methylene blue (MB) dye split when exposed to visible light. The Eu:WO 3 (7 wt%) nanoparticles showed the best photocatalytic property within 120 min. The Eu:WO 3 (7 wt%) nanoparticles showed the maximum antibacterial efficiency against Staphylococcus aureus , with a zone of embarrassment of 19 mm. Overall, the study demonstrates the successful synthesis of Eu-doped WO 3 nanoparticles and their potential applications in photo catalysis and antibacterial activity, with promising results particularly at higher Eu doping concentrations. [ABSTRACT FROM AUTHOR]

The electrophysical properties of nanostructured MgAl2O4 ceramics sintered at 1300 °C for 5 h, as well as thick films were obtained and investigated. The study of adsorption-desorption cycles was carried out after sintering and aging test. It is shown that ceramic has a sensitivity to humidity in the range of 25–95% with minimal hysteresis of the characteristic in adsorption-desorption cycles, which can be eliminated after the aging test. Thick films based on it are characterized by hysteresis and loss of sensitivity at low values of relative humidity, which is caused by the clogging of small nanopores. [ABSTRACT FROM AUTHOR]

This study explores the influence of environmental factors and printing orientation on the aging of additive manufactured polyamide 12 (PA12). A multifactorial experimental design was employed to age specimens under controlled conditions. Analysis of variance revealed that temperature, irradiance, relative humidity, and time significantly impact the ultimate tensile strength (UTS) and Young's modulus (Y) of PA12. Applying multiple linear regression methods produced predictive models with R2 values of 0.9075 for the UTS and 0.5226 for the Y, indicating substantial explanatory power for the specimen's UTS. These models enhance understanding of PA12 aging, aiding in the design of more durable mechanical parts for applications exposed to environmental conditions, such as footwear, automotive components, and medical devices. As next steps, future research could empirically deploy these developed predictive models and explore longer time scales to further elucidate the long‐term aging behavior of additively manufactured PA12. [ABSTRACT FROM AUTHOR]

In this study, biocompatible magnesium oxide (MgO) nanostructures were synthesized using an aqueous solution of Piper betle leaf methanolic extract. The color change during the synthesis process, i.e., colorless to dark brown solution, indicates the formation of MgO nano structures which is further confirmed through UV–Visible spectrum that exhibited characteristic absorption band at 329 nm. Results obtained from morphological analysis reveal that MgO nano flakes (MgO NFs) are present as triangular and polyhedral shapes having an average size ranging between 150 and 200 nm with clear lattice fringes. Secondary metabolites were clearly identified from the FTIR spectrum, and they helped in reduction and stabilization during the synthesis of MgO NFs. The XRD pattern displayed Braggs planes of (111), (220), (220), (311), and (222) with a face centered cubic (FCC) structure, which was further confirmed from the SAED pattern using HRTEM analysis. The as-synthesized MgO NFs manifested profound antimicrobial activity against gram positive as well as gram-negative bacteria with favorable biocompatibility. Furthermore, methylene orange dye was degraded almost completely (98.36 %) in the presence of MgO NFs photo catalysts within 1 h of sunlight illumination. In addition, MgO NFs displayed high level of antioxidant properties with recorded IC 50 value of 15.89 μg/ml. [ABSTRACT FROM AUTHOR]

As the application of polycarbonate (PC) in various fields continues to expand, the requirements for its flame retardancy are becoming increasingly stringent. To enhance the flame retardancy of PC, employing multi‐element synergistic effects and developing novel flame retardants are considered as vital strategies. This work introduces a blend of 1,3‐Benzenedisulfonic acid dipotassium salt (KSP) and three types of phenyl polysiloxanes, namely Octaphenylcyclotetrasiloxane (P4), Octaphenylsilsesquioxane (OPS), and ladder‐like Polyphenylsesquioxane (L‐PPSQ), into PC to create composites. The thermal stability and combustion properties of these composites were characterized using thermogravimetric analysis (TGA), limiting oxygen index (LOI), UL‐94 vertical burning, and cone calorimetry tests. Composites with phenyl polysiloxanes achieved a UL‐94 V‐0 flame retardant rating for 1.6 mm thickness sample and reduced the peak heat release rate by 30%–45%. PC composites with 3% OPS and 0.03% KSP achieved optimal performance, howing a LOI of 34.5%, a 45.4% reduction in peak heat release, and a 40.5% reduction in total smoke release. The flame‐retardant mechanism was analyzed using scanning electron microscopy (SEM), energy‐dispersive X‐ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), and pyrolysis‐gas chromatography‐mass spectrometry (Py‐GC‐MS). [ABSTRACT FROM AUTHOR]

Melt extrusion process was followed in order to improve the high crystallinity and poor toughness of poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) blend materials. It was achieved by the incorporation of epoxy‐terminated hyperbranched polyester (EHBP) elastomer into PHBV and polycaprolactone (PCL). EHBP cross‐links PHBV and PCL through ring‐opening polymerization of epoxy‐terminated and carboxyl groups. The mass percentages of EHBP in the PHBV/PCL blends are 1, 2, 3, and 4mass%, which are expressed as 1, 2, 3, and 4 phr in the following text. Therefore, when the EHBP content was 3 phr, the Young's modulus and tensile strength of the blends are increased to 750 and 15 MPa, respectively, which was comparable to the biodegradable polymers used for packaging. Simultaneously, compatibility between PHBV and PCL has been improved and the particle size reduction of blends can be obviously observed in scanning electron microscope (SEM) images. Dynamic mechanical analysis (DMA) analysis revealed that PHBV and PCL showed improved compatibility with each other by the addition of EHBP. Differential scanning calorimetry (DSC) revealed that the decrease of crystallinity of the blend was consistent with the increase in mechanical properties. Additionally, all the bio‐blends show good thermal stability. Food overall migration studies showed that the amount of migration of composite materials in contact with food was also far lower than the national standard value. Therefore, PHBV/PCL/EHBP blends are expected to be used in the field of food packaging. [ABSTRACT FROM AUTHOR]

Objective(s): Quercetin is a plant flavonoid known for its pharmacological activities, such as antioxidant, anti-inflammatory, and anti-cancer properties. However, there is limited information available regarding its potential toxicities. A previous study showed that quercetin can inhibit human ether-a-go-related gene (hERG, also named KCNH2) currents, which may lead to long QT syndrome, torsade de pointes (TdP), and even sudden cardiac death. This study aimed to investigate the effects of quercetin on hERG and its potential mechanism. Materials and Methods: hERG currents and action potential duration (APD) were assessed using the patch clamp technique. Molecular docking was employed to elucidate the binding sites between quercetin and hERG. Transfection of wild-type or mutant plasmids was used to verify the results of molecular docking. Western blot was performed to determine the expression levels of hERG, transcription factor SP1, molecular chaperones HSP70 and HSP90, phosphorylated E3 ubiquitin ligase p-Nedd4-2, serum- and glucocorticoid-inducible kinase (SGK1), and phosphatidylinositol 3-kinase (PI3K). Immunoprecipitation was conducted to evaluate hERG ubiquitination. Results: Quercetin acutely blocked hERG current by binding to F656 amino acid residue, subsequently accelerating channel inactivation. Long-term incubation of quercetin accelerates Nedd4-2-mediated ubiquitination degradation of hERG channels by inhibiting the PI3K/SGK1 signaling pathway. Moreover, the APD of human induced pluripotent stem cell-derived cardiomyocytes (hiPS-CMs) is significantly prolonged by 30 µM quercetin. Conclusion: Quercetin has a potential risk of proarrhythmia, which provided useful information for the usage and development of quercetin as a medication. [ABSTRACT FROM AUTHOR]

In response to the long-term non-degradation and environmental pollution caused by the use of horizontal plastic drainage boards, a new approach is proposed in this study, which involves employing horizontal straw drainage system under vacuum preloading treatment for dredging sludge. Through laboratory model tests, the results show that horizontal straw drainage system exhibited excellent performance in treating dredged sludge, with an optimal spacing design of 40–60 cm. During the vacuum preloading test, the straw drainage system continuously degraded, and the degradation by-products of straw, in turn, enriched elements like nitrogen, phosphorus, potassium, etc., in the soil. The two processes of the degradation of straw drainage system and the eco-reinforcement of dredged sludge interacted actively with each other. Finally, a new reinforcement method for on-site dredging sludge was proposed by installing layered straw drainage boards. Therefore, straw drainage system was highly recommended for field application, due to their cost-effective and environmentally friendly characteristics. [ABSTRACT FROM AUTHOR]

The present study investigates the effects of the degradation of mechanical properties (pinching, stiffness degradation, and strength degradation) in load-deformation relationship of the superstructures equipped with friction pendulum systems on the seismic fragility and reliability results. An equivalent two-degree-of-freedom model is employed, in which the Bouc-Wen hysteretic model characterizes the inelastic behavior of both the superstructure and the isolator. To examine a wide variety of system combinations with different structural properties and degradation severity, a comprehensive parametric study is performed. Incremental dynamic analyses are carried out to develop fragility functions. Subsequently, the seismic reliability of both the superstructure and the isolation level is assessed. Results indicate that the negative effects of degrading behavior are more prominent in stiff superstructures as it significantly decreases structural capacity and reliability indices. It is demonstrated that the system is primarily influenced by pinching behavior rather than degradation in strength and stiffness, especially at low intensity levels that correspond to lower limit-states. In the majority of investigated systems, the seismic demand in the isolator decreases when superstructures undergo degrading behavior. Overall, such effects should be considered in the reliability-based design procedure to attain design consistency in terms of reliability. The results of this paper that account for the degrading effects enable reliable estimations of key parameters essential for the design of the superstructure and the isolator. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: The saline and buffered environment in actual wastewater imposes higher demands on Fenton and Fenton‐like catalytic systems. This study developed a MoS2 co‐catalytic Fe2O3 Fenton‐like system with controllable Lewis acid‐base sites, achieving efficient treatment of various model pollutants and actual industrial wastewater under neutral buffered environment. The acidic microenvironment structured by the edge S sites (Lewis basic sites) in the MoS2/Fe2O3 catalyst is susceptible to the influence of Lewis acidic sites constructed by Mo and Fe element, affecting catalytic performance. Optimizing the ratio of precursor amounts ensures the stable presence of the acidic microenvironment on the surface of catalyst, enabling the beneficial co‐catalytic effect of Mo sites to be realized. Furthermore, it transcends the rigid constraints imposed by the Fenton reaction on reaction environments, thereby expanding the applicability of commonplace oxides such as Fe2O3 in actual industrial water remediation. [ABSTRACT FROM AUTHOR]

The sustainability and feasibility of using visible irradiation in photocatalysis is a promising approach for water purification. In this study, photocatalytic degradation of a widely used analgesic and antipyretic drug, acetaminophen (ACM), with metal-loaded an efficient photocatalyst (TiO 2 NPs-Co/Polycalix (Christen et al., 2010) [4]resorcinarene (TCP)) was inv estigated using visible light. photocatalyst structural, surface, and morphological features were characterized using FTIR, XRD, TEM, EDX, PL, and DRS analyses. Considering various sites of Polycalix (Christen et al., 2010) [4]resorcinarene in the TCP, studied by trapping experiments. A novel charge transfer bridge for electron-hole recombination is made possible by using Co and TiO 2 as electron transfer mediators with electronic conductivity. This results in efficient process and energy optimization, which makes it easier for ACM to degrade throughout the absorption process. The ACM (15 and 40 mg/L) achieved complete degradation under visible light irradiation with 0.6 g/L of TCP at pH = 5.0 during 120 min reaction because of the good synergetic effect of the catalyst systems. Additionally, the intermediates generated by photo electrocatalytic activities were identified, and two potential paths for degradation were suggested. Some of these organic products were identified by High-Performance Liquid Chromatography (HPLC). [ABSTRACT FROM AUTHOR]

Textile dyeing releases over 80% of industrial effluents without proper treatment. Dye discharged into effluents typically needs degradation before release into aquatic environments. In this regard, the present paper reports the nanocomposite copper oxide/polyaniline (CuO/PANI) is successfully synthesized by in situ chemical oxidative polymerization method and investigates their catalytic activity against organic dyes and nitro compounds. CuO is synthesized by colloidal sol–gel method using oxalic acid as capping agent to obtained desired morphology. The elemental composition, unit cell and lattice parameters of nanocomposite are characterized by using XRD. The XRD revealed that nanoparticles are extremely crystalline, but nanocomposite is amorphous because of the presence of polymer. The structural and elemental analysis of CuO and CuO/PANI is confirmed by SEM and EDX analysis. FTIR spectra of CuO showed bending vibration, while CuO/PANI showed the presence of benzenoid and quinoid rings. Catalytic productivity of the CuO and CuO/PANI as catalysts in degradation of dyes and reduction of nitro compounds is also studied. The degradation and reduction processes are monitored through the utilization of UV–Vis spectrophotometer. The catalytic activity of both catalysts is evaluated by several parameters including kapp, degradation/reduction time, % degradation/reduction, degraded/reduced concentration and half-life. Among all substrates, highest kapp is 0.0653 min−1 for CV by CuO, while 0.0502 min−1 for EBT by CuO/PANI due to large surface area. On degradation and reduction rate of substrates, the impact of functional group type and orientation, bond type and steric hindrance is also investigated. [ABSTRACT FROM AUTHOR]

Acidic conditions affect the archaeological bone in the burial and in uncontrolled display and storage environment or due to improper restoration processes. Accordingly, bones become weak and fragile. This study aims to evaluate nano calcium propionate and nano styrene butyl acrylate (used for the first time in the treatment of bones) at different concentrations for deacidification and consolidation of fragile bones. New bone samples were prepared. Artificial accelerated aging (acid and heat) was applied to prepare aged untreated samples. Deacidification and consolidation processes using the materials mentioned above were applied. The analytical techniques used were transmission electron microscope (TEM) and thermal gravimetric analysis (TGA) were used for morphological and thermal stability investigation for the prepared nano styrene butyl acrylate copolymer and its calcium propionate nonocomposites, a digital microscope and scanning electron microscope (SEM) for investigation of the surface morphology, pH value measurement, change of color measurement, attenuated total reflection—Fourier transform infrared spectroscopy (ATR/FTIR), contact angle (wettability), and X-ray diffraction analysis for measurement of bone crystallinity. The results proved that acid-heat aging affected bone properties such as changes in surface morphology and color, decrease in pH value, and contact angle. Bone samples became more crystalline, and the chemical composition of bone was also affected. The treatment of aged untreated bone samples with the materials used in this study improved their properties, such as increasing the pH value and contact angle. The surface morphology, color change, and crystallinity of bone improved and became more stable. [ABSTRACT FROM AUTHOR]

With the increasing focus on sustainable development, the exploration of renewable and environmentally friendly resources for product synthesis has become paramount. This study aims to investigate the production of dihydroxystearic acid through the in situ hydrolysis of epoxidized oleic acid. Epoxidation of oleic acid was achieved through the utilization of in situ generated performic acid, resulting in the production of epoxidized oleic acid. The synthesis of performic acid involved the combination of formic acid as an oxygen carrier and hydrogen peroxide as an oxygen donor. A maximum epoxide yield of 65% was attained at an optimum reaction time of 30 min. Hydrochloric acid was found to be the most efficient catalyst. A kinetics study was also done using the genetic algorithm to find the reaction rate of dihydroxystearic acid production. The difference between simulation and experimental results was less than 0.1%, which is insignificant. The findings highlight the potential of utilizing renewable resources for the synthesis of high-value compounds, promoting a greener and more sustainable future. [ABSTRACT FROM AUTHOR]

The combination of plasma technology with microfluidics has gained significant attention in recent years. The unique characteristics of microfluidic chips, such as high surface-to-volume ratio and efficient mass transfer, coupled with plasma's ability to provide the necessary green energy for the degradation of complex molecules, make this combination promising for water and wastewater treatment applications. A gas/liquid biphasic dielectric barrier discharge (DBD) plasma microreactor powered by a nano-pulsed excitation source, at atmospheric pressure, was used to study the degradation of p-benzoquinone and caffeine in water, chosen as model molecules for water pollution. Based on High Performance Liquid Chromatography (HPLC) analyses, the argon plasma was able to completely degrade both molecules at concentrations 10− 5, 10− 4 and 10− 3 mol/L. At higher concentration (10− 2 mol/L), the plasma promotes the synthesis of hydroquinone from p-benzoquinone. A 50% mineralization is achieved after plasma for the caffeine in aqueous solution at 10− 5 M. [ABSTRACT FROM AUTHOR]

Wastewater generated by the textile industry contains a variety of harmful and complex substances. These effluents can negatively impact aquatic ecosystems and human health if not managed properly. The textile industry relies on various chemicals and water to dye and wash fabric. The textile effluent exhibits vibrant colours, elevated pH levels, increased temperature, and higher COD levels. Various factors contribute to the increased pollutant load in effluents, including diluted solids, suspended particles, colours, and toxic metals. Various techniques are used to address textile wastewater, including mechanical, chemical, biological, hybrid, and advanced oxidation methods. This study offers a thorough examination of the dyes and chemicals utilized in the textile industry. It specifically looks at various treatment methods for removing pollutants from industrial wastewater, including chemical, biological, physical, AOPs, and hybrid systems. The findings suggest that photocatalytic techniques are the most effective in terms of rapid dye removal, cost-effectiveness, timeliness, and environmental friendliness. This review also offers a detailed analysis of the past decade and explores the challenges and potential of this innovative approach in the context of sustainable development. [ABSTRACT FROM AUTHOR]

The degradation of carbendazim (CBZ) through TiO2 photocatalysis, in the presence of halide ions and under near-UV light irradiation, was investigated. HPLC–MS technique was used to characterize the photoproducts. Spectrophotometric analysis showed that CBZ degraded slowly in TiO2 aqueous dispersions containing no salt (CBZ conversion of 6% after ca. 5 h of irradiation). The photodegradation efficiency increased particularly by addition of bromide salts. Indeed, CBZ reached complete degradation after ca. 30 min at the maximum concentration of NaBr used (0.05 M). Two significant aspects have emerged from the data analysis: the bromide role is to cause inhibition of the electron–hole recombination, a reaction known to be competitive with the reactive process; CBZ photodegradation is especially initiated by direct hole transfer pathway, whereas the OH• role is crucial in the catalyst regeneration process. Degradation attempts under sunlight appeared promising for a more sustainable photocatalytic process. [ABSTRACT FROM AUTHOR]

There are obstacles to the widespread use of small electric vehicles (EVs) in Rwanda, including concerns regarding the battery range and lifespan. Lithium-ion batteries (LIBs) play an important role in EVs. However, their performance declines over time because of several factors. To optimize battery management systems and extend the range of EVs in Rwanda, it is essential to understand the influence of the driving profiles on lithium-ion battery degradation. This study analyzed the degradation patterns of a lithium-ion battery cell that propels an E-bike using various real-world E-bike driving cycles that represent Rwandan driving conditions under deep discharge (> 80 %). By being aware of these variables, battery failure can be slowed and improved battery performance can be achieved to promote the transition to cleaner transportation in Rwanda for the productive use of energy. The analyzed parameters that affect battery performance are temperature, driving cycles, and state of charge. It was found that the higher the temperature, the higher was the rate of fading. On the other hand, the EVs that operate in the region with higher elevation (hilly region) combined with a flat surface where the riders use their physical forces to propel the E-bike and their batteries lose their capacity rapidly compared to those operating in regions where the energy from the lithium-ion battery assists for the entire mileage. By draining the battery to 10% and charging it to 90% of its initial capacity, the capacity fading decreased by 5%. [ABSTRACT FROM AUTHOR]

In response to the escalating need for nanomaterials characterized by enhanced properties and reduced environmental impact, this study addresses critical challenges associated with conventional nanomaterial synthesis methods, particularly focusing on concerns related to environmental toxicity and economic feasibility. In this study, we report the eco-friendly synthesis of silver-zinc oxide nanocomposites using leaf extracts of Quassia indica (QI- Ag: ZnO NC). The synthesized QI- Ag: ZnO nanocomposites were characterized using various techniques including UV-visible spectroscopy, X-ray diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Dynamic Light Scattering (DLS), Field-Emission Scanning Electron Microscopy (FE-SEM) with Energy Dispersive X-ray Spectroscopy (EDX), High Resolution Transmission Electron Microscopy (HR-TEM), and Selected Area Electron Diffraction (SAED). The photocatalytic activity of the biosynthesized QI- Ag: ZnO NC was evaluated against several textile dyes. Reactive Blue-220 exhibited the highest percentage of degradation (99.97%), closely followed by Reactive Blue-222 (99.37%), while Reactive Red-120 displayed significant degradation (94.62%). Remarkably, these nanocomposites exhibited significant photocatalytic degradation of the tested dyes, suggesting their potential application in wastewater treatment for dye removal. Furthermore, phytotoxicity studies were conducted to assess the impact of the nanocomposites on plant growth and brine shrimp mortality. To evaluate their cytotoxicity, the nanocomposites synthesized were assessed using the MTT assay on MCF-7 and MDA-MB-231 cancer cells. These findings suggest that QI- Ag: ZnO NCs have promising applications in environmental remediation and cancer therapy, opening avenues for further advancements in the arena of nanomaterial synthesis and utilization. [ABSTRACT FROM AUTHOR]

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The use of bioplastics is a new strategy for reducing microplastic (MP) waste caused by petroleum‐based plastics. This problem has received increased attention worldwide, leading to the development of large‐scale bioplastic plants. The large amount of MPs in aquatic and terrestrial environments and the atmosphere has raised global concern. This article delves into the profound environmental impact of the increasing use of petroleum‐based plastics, which contribute significantly to plastic waste and, as a consequence, to the increase in MPs. We conducted a comprehensive analysis to identify countries that are at the forefront of efforts to produce bioplastics to reduce MP pollution. In this article, we explain the development, degradation processes, and research trends of bioplastics derived from biological materials such as starch, chitin, chitosan, and polylactic acid (PLA). The findings pinpoint the top 10 countries demonstrating a strong commitment to reducing MP pollution through bioplastics. These nations included the United States, China, Spain, Canada, Italy, India, the United Kingdom, Malaysia, Belgium, and the Netherlands. This study underscores the technical and economic obstacles to large‐scale bioplastic production. Integr Environ Assess Manag 2024;20:1892–1911. © 2024 SETAC Key Points: Microplastics (MP) have caused concern due to their environmental effects, potential to release plastic monomers, affinity for chemical interactions, and potential to enter aquaculture and fishery production.The findings pinpoint the top 10 countries demonstrating a strong commitment to reducing MP pollution by replacing petroleum‐based plastics with bioplastics.Using bibliometric techniques, we mapped and identified the countries that were most actively engaged in shifting to bioplastic production during the period 2001–2021.This article focuses on starch‐based bioplastics used primarily in food packaging, increasing their mechanical properties by adding fibers, and extending the shelf life of food with antibacterial nanoparticles. [ABSTRACT FROM AUTHOR]

Citrinin (CIT) is a nephrotoxic mycotoxin, produced by several species of Penicillium, Aspergillus, and Monascus. The foodstuffs most frequently contaminated with CIT include cereals, cereal products, and red yeast rice. Studies on the occurrence of CIT in food have shown that the CIT concentrations in processed cereal-based products are generally lower than in unprocessed industry cereal samples. One possible explanation is the reaction of CIT with major food components such as carbohydrates or proteins to form modified CIT. Such modified forms of CIT are then hidden from conventional analyses, but it is possible that they are converted back into the parent mycotoxin during digestion. The aim of this study is therefore to investigate reactions of CIT with food matrix during thermal processes and to gain a deeper understanding of the degradation of CIT during food processing. In this study, we could demonstrate that CIT reacts with amino compounds such as proteins, under typical food processing conditions, leading to modified forms of CIT. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: The saline and buffered environment in actual wastewater imposes higher demands on Fenton and Fenton‐like catalytic systems. This study developed a MoS2 co‐catalytic Fe2O3 Fenton‐like system with controllable Lewis acid‐base sites, achieving efficient treatment of various model pollutants and actual industrial wastewater under neutral buffered environment. The acidic microenvironment structured by the edge S sites (Lewis basic sites) in the MoS2/Fe2O3 catalyst is susceptible to the influence of Lewis acidic sites constructed by Mo and Fe element, affecting catalytic performance. Optimizing the ratio of precursor amounts ensures the stable presence of the acidic microenvironment on the surface of catalyst, enabling the beneficial co‐catalytic effect of Mo sites to be realized. Furthermore, it transcends the rigid constraints imposed by the Fenton reaction on reaction environments, thereby expanding the applicability of commonplace oxides such as Fe2O3 in actual industrial water remediation. [ABSTRACT FROM AUTHOR]

This study aimed to evaluate the nitrogen fertilisation supply method on wheat silage fermentation parameters and nutritional value. Eighteen experimental plots were used in a randomised block design to assess the following treatments: (1) control (CON): crop without nitrogen fertilisation; (2) surface (SUR): 100 kg/ha N during the crop, applied in surface; (3) furrows (FUR): 100 kg/ha N during the crop, applied in furrows during the seeding. Whole plants were manually harvested at 5 cm height 83 days after the sowing. One experimental silo (PVC tubes) was produced for each agronomical plot and stored for 69 days. In general, N fertilisation did not affect silage pH and ammonia-N (NH3-N) content, but silos FUR had less NH3-N than those with SUR. Fertilisation increased the CP and DM content and reduced starch in the silage. FUR increased DM and reduced CP compared to SUR. Furthermore, N fertilisation increased non-protein nitrogen and decreased in vitro degradation of DM and OM. Fertilisation methods did not affect N fractions in silage or in vitro degradation. Therefore, N fertilisation, especially FUR, reduces NH3-N and CP and increases DM content of silage, but decreases in vitro DM and OM degradation. [ABSTRACT FROM AUTHOR]

This study explores the impact of ageing factors – i.e., perspiration, disinfection procedures and ultraviolet radiation – on the structural and performance characteristics of novel viscoelastic polyurethane foams specifically developed for use in seals for respiratory protective devices (RPDs). The investigation includes an analysis of resilience, compression set and recovery time to ascertain the influence of the chosen factors on the foam’s mechanical properties. Furthermore, an in-depth exploration of the foams’ thermal properties and chemical structure was carried out using thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR), respectively. The influence of the ageing factors on the foams’ microstructure was scrutinized via scanning electron microscopy (SEM), supplemented by assessments of colour change and contact angle alterations. The experimental results were contextualized within the existing literature, with particular attention to the desired attributes of RPD seals composed of these newly engineered materials. Recommendations for use were then formulated. [ABSTRACT FROM AUTHOR]

2D hybrid organic–inorganic perovskites are potentially promising materials as passivation layers that can enhance the efficiency and stability of perovskite photovoltaics. The ability to suppress ion transport is proposed as a stabilization mechanism, yet an effective characterization of relevant modes of halide diffusion in 2D perovskites is nascent. In light of this knowledge gap, molecular dynamics simulations with enhanced sampling and experimental validation to systematically characterize how ligand chemistry in seven (R‐NH3)2PbI4 systems impacts halide diffusion, particularly in the out‐of‐plane direction is combined. It is found that increasing stiffness and length of ligands generally inhibits ion transport, while increasing ligand polarization generally enhances it. Structural and energetic analyses of the migration pathways provide quantitative explanations for these trends, which reflect aspects of the disorder of the organic layer. Overall, this mechanistic analysis greatly enhances the current understanding of halide migration in 2D hybrid organic–inorganic perovskites and yields insights that can inform the design of future passivation materials. [ABSTRACT FROM AUTHOR]

Recently, metal-supported solid oxide fuel cells (MS–SOFCs) have been in the spotlight again for their design, thanks to their inexpensive materials, robustness, resistance to thermal cycling, and benefits of manufacturability. Hydrogen energy electrochemical devices, like MS–SOFCs, have a lot of potential. They are very ideal substitutes for solid oxide fuel cells (SOFCs) that utilize electrolytes or ceramic electrodes as their carrier basis, because of their greater durability, mechanical stability, heat cycle resistance, and rapid startup time. Even though MS–SOFCs have several advantages over conventional ceramic-based SOFCs, researchers are still struggling to perfect them due to issues such as selecting the appropriate metal-based material for the electrodes (anode, electrode) and comprehending how they deteriorate. This limitation might be evaded by optimizing the pore former filling and the diameter of the metallic supports (130–250μm). Optimization methods, such as particle swarm optimization, as well as penetration cycle numbers (1–15), as well as the impacts of fire temperatures (400–900∘C), were investigated to aid in optimizing the catalyst infiltration procedure. The enhanced cell outperformed its original performance by a factor of three, reaching an ideal energy density of 0.9W cm−2 at 700∘C when powered by hydrogen. The improved cells had a 2% degradation rate per 100h at 550∘C, a 4.5% degradation rate at 600∘C, and a 5.5% degradation rate at 700∘C. We used electrochemical impedance spectroscopy and scanning electron microscopy to look at the catalyst’s mass shipping, coarsening, and chromium poisoning. [ABSTRACT FROM AUTHOR]

AbstractRadioisotope thermoelectric generator (RTG) technology has a very long and incredibly successful history of providing heat and power to some of humankind’s most successful space exploration missions. Members of the community that support and maintain this technology often like to show the entire history of RTG performance on “The Graph.” Meant to impress, The Graph does its job in that regard. Unless you were connected to the right people, however, it was very difficult to get a copy of The Graph or its underlying data. This made it difficult for many to dive into the technical details or evaluate individual RTG performance from historical missions. To make matters worse, the performance for several missions in The Graph were incomplete. In 2020, with a little extra time on their hands thanks to COVID, the authors reached throughout the RTG community to locate and collate the missing RTG data. This information was then published as an open-source tabular Dataset. Users can now build their own version of The Graph or use the data for a more detailed analysis of RTG performance. Updates to the currently operating missions in The Dataset are expected to occur on a roughly annual basis. This Dataset represents the most comprehensive, authoritative, up-to-date repository of all RTG performance available today. [ABSTRACT FROM AUTHOR]

Long‐chain polyamides (polyethyleneamides) were prepared from polyethylenes bearing in‐chain carbonyl groups (polyethyleneketones) by the oxime formation and successive Beckmann rearrangement. (Diethylamino)sulfur trifluoride (DAST) was utilized as a promoter, which allowed mild conversion of the oxime group in spite of low solubility of the polymers. The polyethyleneamide exhibited different tensile property compared to a commercial HDPE. [ABSTRACT FROM AUTHOR]

Introduction: Lung cancer is the leading cause of cancer-related death worldwide. The treatment for lung cancer, particularly for non-small cell lung cancer (NSCLC), remains a clinical challenge. Cancer stem cells are vital for lung cancer development. This study aimed to determine the influence of the neuronally expressed developmentally downregulated 4-fibronectin leucinerich transmembrane 2 (NEDD4-FLRT2) axis on cancer cell stemness in NSCLC. Methods: FLRT2 expression in NSCLC tissues and stem cells was investigated using western blot and RT-qPCR. The sphere formation assay and the abundance of stemness markers were employed to confirm the stemness of NSCLC stem cells. The CCK-8, colony formation, and Trans-well assays, as well as flow cytometry, were used to determine NSCLC stem cell growth, metastasis, and apoptosis, respectively. The Co-IP assay was used to confirm the binding between NEDD4 and FLRT2. Xenograft tumor mouse models were used to investigate tumorigenesis in vivo. Results: Here, we reported that FLRT2 expression was reduced in NSCLC tissues, cells, and NSCLC stem cells. FLRT2 upregulation inhibited NSCLC stem cell proliferation, sphere formation, and drug resistance and promoted drugresistant cell apoptosis. Furthermore, FLRT2 overexpression demonstrated antitumor effects in a xenograft tumor mouse model. Mechanically, FLRT2 was ubiquitinated and degraded by E3 ligase NEDD4. NEDD4 overexpression significantly abolished the inhibitory effects of FLRT2 on NSCLC stemness, as evidenced by in vitro and in vivo experiments. Discussion: This study revealed that FLRT2 acted as a tumor suppressor by inhibiting cancer cell stemness in NSCLC. NEDD4 promoted ubiquitination degradation of FLRT2 protein. NEDD4 counteracted the inhibitory effects of FLRT2 on NSCLC stem cell tumorigenesis. [ABSTRACT FROM AUTHOR]

Firefighters rely on their protective clothing as a second skin to perform their job. In the middle of this multilayered protective garment, the moisture barrier plays a vital role in preventing liquids to enter while allowing perspiration to escape. This research delves into the impact of accelerated ultraviolet (UV) aging on the performance of firefighter protective clothing moisture barriers, focusing on tear force retention, water vapor transmission rate (WVTR), and wetting via apparent contact angle. Changes in the tearing behavior and reductions in the tear force and tearing distance were observed after aging. Additionally, a reduction in WVTR was found for all the moisture barriers, due to pore closure in the ePTFE/FR PU membrane. In terms of water repellency, the base fabric side of one moisture barrier experienced a transition from hydrophobic to superhydrophilic potentially due to the degradation of the water‐repellent finish. The investigation also revealed that, due to the screening effect by the outer shell fabric, only a low percentage of UV radiation received by the turnout gear, less than 2% in the UVA range, may reach the moisture barrier. These results indicate the need to consider realistic exposure scenarios when assessing moisture barrier service life. [ABSTRACT FROM AUTHOR]

Computed tomography (CT) is an excellent tool to solve certain engineering problems connected to material science (such as sulfate swelling, internal degradation due to freezing, and alkali silicate swelling) and to understand specific processes (frost peeling, acid action). Albeit borne and mostly used in the medical domain, CT is increasingly used in the examination of the internal structure of building materials, where degradation processes occur to the detriment of their mechanical performance and durability. This paper presents five engineering problems concerning concrete freezing and thawing, concrete at high temperatures, timber charring, spalling in asbestos‐cement pipes, and deterioration in prestressed concrete pipes due to the corrosion of metallic inserts. In each case, the degradation processes are monitored via CT, something that may be crucial in the renovation and preservation of historical structures. [ABSTRACT FROM AUTHOR]

Among the perovskite oxide community, La‐based perovskites have garnered considerable interest due to their remarkable properties including catalytic, electrocatalytic, photocatalytic, sensing, electrical, magnetic, and optical characteristics. Herein, rhodamine‐B (RB) dye has been reported to be sono‐catalytically decomposed by an ultrasound‐assisted advanced oxidation process (AOP) using perovskite‐type LaMnO3 (LMO) nanospheres synthesized via ultrasonic approach. Several physiochemical characterizations such as XRD, FT‐IR, XPS, SEM, TEM, and SEM‐EDS investigations were used to investigate the LMO perovskite nanospheres. Then, LMO potential for adsorption and the sonocatalytic decolorization of RB dye in an aqueous solution are examined. With LMO perovskites, the adsorption and removal kinetics of RB correspond to the pseudo‐first‐order model. Furthermore, by utilizing the pseudo‐first‐order, the RB dye process is removed with improved efficacy in the following sequence: Agitation alone: 3.76×10−4 min−1

The escalating demand for plastics has resulted in a surge of plastic waste worldwide, posing a monumental environmental challenge. To address this issue, a versatile photo‐oxidative degradation method applicable to seven distinct polymer families is proposed, comprising poly(isobutyl vinyl ether) (PIBVE), poly(2,3‐dihydrofuran) (PDHF), poly(vinyl acetate) (PVAc), poly(n‐butyl acrylate) (PBA), poly(methyl acrylate) (PMA), poly(vinyl chloride) (PVC), poly(dimethyl acrylamide) (PDMA), poly(ethylene oxide) (PEO), poly(oligo(ethylene glycol) methyl ether acrylate) (PEGMEA), and even poly(methyl methacrylate) (PMMA). This method employs photo‐mediated hydrogen atom transfer (HAT) followed by oxidation to promote polymer degradation. This reaction is carried out under aerobic condition in the presence of iron trichloride (FeCl3) as a photocatalyst in combination with low‐intensity purple light irradiation. The process can degrade up to 97% of the polymer in less than 3 h. This degradation process can be easily controlled by switching the light off, which allows for precise modulation of the degradation rate, enhancing the effectiveness of the method. Overall, this method provides a sustainable method for degrading various polymer types with low energy input. [ABSTRACT FROM AUTHOR]

The role of tin fluoride in defining the complex surface chemistry of tin halide perovskites (THP) is investigated. It is shown that oxygen is found on the surface of tin perovskite thin films even if prepared under a virtually inert environment; however, the presence of SnF2 strongly affects the chemical nature of the found species. Oxygen primarily binds to tin in the form of SnO2 only when SnF2 is added to the precursor solution, while it preferentially binds to carbon and hydrogen in pristine materials. Thanks to the spatial mapping of both the local chemical environment and photoluminescence, it is shown that pristine films have a higher accumulation of iodine at the grain boundaries while the addition of SnF2 allows for preserving the perovskite phase and reducing chemical and optical heterogeneities. Finally, SnF2 does not help in avoiding nor slowing down the degradation of the perovskite film when exposed to ambient air and oxidation occurs on the whole THP‐grain surface. These results provide insightful guidance toward understanding oxidation in THPs and elucidate its detrimental effect on the material's properties. [ABSTRACT FROM AUTHOR]

The fabrication of hydroxyapatite (HAP)/MgO composite coatings on Mg alloy is crucial for enhancing the corrosion resistance and biocompatibility of biomedical implants. In this study, we aimed to investigate the effects of two different surface modification methods, i.e., electrochemical (electrodeposition, ED) and chemical (solution treatment, ST), on the phase structure, degradation properties, and biocompatibility of the composite coatings in comparison to the anodized coating. The surface morphologies and crystalline structures of the coatings were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). Subsequently, the degradation rate of the coatings in simulated body fluid were comprehensively evaluated by using electrochemical impedance spectroscopy (EIS), potentiodynamic polarization and scanning electrochemical microscopy (SECM) tests. Additionally, in-vitro cell proliferation assays were employed to quantitatively assess the biocompatibilities of the coatings. The results showed that both ED and ST methods were effective in depositing HAP on anodized Mg alloy, resulting in different surface morphologies with hydroxyapatite layer thicknesses of 2.71 μm and 3.56 μm, respectively. In this way, the HAP-deposited coatings exhibited improved corrosion resistances and biocompatibilities compared with those of the anodized coating. Specifically, the ST-deposited composite film displayed superior degradability and biocompatibility which was attributed to its filiform surface morphology and thicker HAP layer. Overall, the present study demonstrates the potential of HAP/MgO composite coatings for biomedical applications, with implications for the development of advanced implant materials with improved performance and biocompatibility. [ABSTRACT FROM AUTHOR]

Excessive use of tetracycline (TC) is alarming owing to its increased detection in water systems. In this study, a photocatalyst was developed to degrade TC using a Ce-N-co-doped AC/TiO2 photocatalyst, denoted as Ce/N-AC/TiO2, prepared using the sol–gel method assisted by microwave radiation, speeding up the synthesis process. Ce/N-AC/TiO2 achieved maximum TC degradation of 93.1% under UV light with optimum sorption system conditions of an initial concentration of 10 mg L−1, pH 7, and 30 ℃, under 120 min. Scavenger experiments revealed that holes and superoxide radicals were the active species influencing the photodegradation process. The TC degradation was appropriately fitted with Langmuir isotherms and a pseudo-second-order (PSO) kinetic model. The change in enthalpy (ΔH) (2.43 kJ mol−1), entropy (ΔS) (0.024 kJ mol−1), and Gibbs free energy (ΔG) (− 4.941 to − 5.802 kJ mol−1) suggested that the adsorption process was spontaneous, favourable, and endothermic. Electrostatic interaction, hydrogen bonding, pore-filling, cationic-π, n-π, and π-π interaction were among the interactions involved between TC and Ce/N-AC/TiO2. Furthermore, Ce/N-AC/TiO2 stability was confirmed through 80% removal efficiency even after the fifth reuse cycle. Notably, this work provides new insight into the production of efficient, reusable, and enhanced photocatalysts using a rapid and cost-effective microwave-assisted synthesis process for pollutant remediation. [ABSTRACT FROM AUTHOR]

Wood–plastic recycled composite (WPRC) are composites obtained by heating and mixing the main raw material, wood flour, with thermoplastic resin, containing at least 40% by mass of recycled material in the raw material. In order to promote the multiple-recycling of WPRC to reduce greenhouse gas emissions and ensure the sustainability of resources, three types of WPRC decking materials with different exposure conditions (outdoor-exposed product, unexposed product and product stored in the factory for a long time) and samples after accelerated weathering tests (WPRC and recycled plastics from raw materials) were evaluated and compared by a TG-DTA in order to develop a method for evaluating the degree of degradation of used WPRC. Exothermic behavior with weight loss was observed in the temperature range of 30–500 °C for the WPRC product in two temperature ranges. In order to focus on the change in the first exotherm by oxidative degradation, where the rapid weight loss begins, this paper will focus on the exothermic behavior that develops in the temperature range of 150–300 °C on the lower temperature side. The results obtained are as follows. (1) Initial oxidation temperature (IOT) measurement from DTA behavior suggested that it is possible to evaluate the degree of degradation of WPRC. (2) On the exposed surface of WPRC exposed outdoors for more than 9 years and 8 months, significant decreases in the IOT were observed up to 1 mm from the surface, and a slight decrease in the IOT was observed between 1 and 2 mm from the surface. On the other hand, for the indoor long-term storage of 11 years and 6 months, there were almost no changes in the IOT with respect to the depth from the surface. Regarding the outdoor long-term-exposed WPRC, significant decreases in the IOT were observed not only on the exposed surface but also on the hollow and ribbed surfaces up to a depth of 1 mm from the surfaces. (3) A similar decrease in the IOT with increasing accelerated degradation time was observed for the WPRC and raw recycled plastic samples after accelerated weathering tests as for outdoor exposure. Furthermore, FTIR-ATR spectra also revealed that accelerated degradation caused oxidative degradation of the plastic. Therefore, it is thought that the decrease in the IOT can be used as an indicator to evaluate the degree of degradation of the plastic raw material in WPRC. [ABSTRACT FROM AUTHOR]

In recent years, significant attention has been paid to the research of light‐ and elevated‐temperature‐induced degradation (LeTID) in silicon solar cells due to the substantial power loss and instability it causes. It has been discovered that the presence of hydrogen is closely linked to the occurrence of LeTID. In this study, a thorough review and re‐assessment of previously published results is conducted and connected with newly obtained data. The findings indicate a complex interaction between different hydrogen complexes and the LeTID defect states. The precursor of LeTID is connected to molecular hydrogen (H2), while the LeTID degradation and regeneration are related to the binding of atomic hydrogen to the precursor and defect, respectively. A detailed description of the various reactions that occur under illumination and in the dark is provided. Additionally, explanation is given on how pre‐annealing can significantly affect the kinetics of LeTID during subsequent light soaking. Furthermore, a comprehensive hydrogen model that incorporates these various reactions and demonstrates an agreement between simulation and experimental results is developed. Finally, the implications of the findings on strategies for mitigating LeTID are discussed. [ABSTRACT FROM AUTHOR]

A rhizosphere strain, Achromobacter insolitus LCu2, was isolated from alfalfa (Medicago sativa L.) roots. It was able to degrade of 50% glyphosate as the sole phosphorus source, and was found resistant to 10 mM copper (II) chloride, and 5 mM glyphosate–copper complexes. Inoculation of alfalfa seedlings and potato microplants with strain LCu2 promoted plant growth by 30–50%. In inoculated plants, the toxicity of the glyphosate–copper complexes to alfalfa seedlings was decreased, as compared with the noninoculated controls. The genome of A. insolitus LCu2 consisted of one circular chromosome (6,428,890 bp) and encoded 5843 protein genes and 76 RNA genes. Polyphasic taxonomic analysis showed that A. insolitus LCu2 was closely related to A. insolitus DSM23807T on the basis of the average nucleotide identity of the genomes of 22 type strains and the multilocus sequence analysis. Genome analysis revealed genes putatively responsible for (1) plant growth promotion (osmolyte, siderophore, and 1-aminocyclopropane-1-carboxylate deaminase biosynthesis and auxin metabolism); (2) degradation of organophosphonates (glyphosate oxidoreductase and multiple phn clusters responsible for the transport, regulation and C–P lyase cleavage of phosphonates); and (3) tolerance to copper and other heavy metals, effected by the CopAB–CueO system, responsible for the oxidation of copper (I) in the periplasm, and by the efflux Cus system. The putative catabolic pathways involved in the breakdown of phosphonates are predicted. A. insolitus LCu2 is promising in the production of crops and the remediation of soils contaminated with organophosphonates and heavy metals. [ABSTRACT FROM AUTHOR]

Firefighters' protective clothing rely on moisture barriers to safeguard against liquid ingress while enabling sweat evaporation for comfort and safety. However, these moisture barriers can degrade over time, jeopardizing firefighters' safety. Existing evaluation methods, primarily visual inspection, are inadequate for assessing moisture barrier integrity in service. This study examines the effect of accelerated hydrothermal aging on the tear force, water vapor transmission rate (WVTR), and apparent contact angle in three moisture barrier models used in firefighter protective clothing. The moisture barriers studied varied in composition, structure, and base fabric fiber content. Results revealed that moisture barriers' responses to aging are influenced by factors, such as fabric structure, adhesive configuration, finish, and the presence of additional coatings. The hardening of the adhesive layer between the ePTFE membrane and the base fabric was observed in two of the moisture barriers, leading to a slight tear force reduction. Two of the moisture barriers also experienced crack and pit formation on the membrane side, which affected the WVTR. The water‐repellent finish on the fabric side degraded in one moisture barrier. Understanding these complex behaviors is essential for predicting the long‐term moisture barrier performance and enhancing firefighter safety. [ABSTRACT FROM AUTHOR]

Since the first isolation of graphene, the importance of van der Waals (vdW) interactions has become increasingly recognized in the burgeoning field of layered materials. In this work, infrared nanoimaging techniques and theoretical modeling are used to unravel the critical role played by interfacial vdW interactions in governing the stability of violet phosphorus (VP)—a recently rediscovered wide bandgap p‐type semiconductor—when exfoliated on different substrates. It is demonstrated that vdW interactions with the underlying substrate can have a profound influence on the stability of exfoliated VP flakes and investigate how these interactions are affected by flake thickness, substrate properties (e.g., substrate hydrophilicity, surface roughness), and the exfoliation process. These findings highlight the key role played by interfacial vdW interactions in governing the stability and physical properties of layered materials, and can be used to guide substrate selection in the preparation and study of this important class of materials. [ABSTRACT FROM AUTHOR]

Plastic pollution is the challenging problem of the world due to usage of plastic in daily life. Plastic is essential for packaging food and other goods and utensils to avoid the risk of microbial attack. Due to its hydrophobic nature, it is used for wrapping as laminates or packaging liquid substances in pouches and sachets. The tensile strength of the plastic is more therefore it is used for manufacturing carrying bags that can bear heavy loads. Plastic is available in various forms as per the requirements in our daily life. Annually millions to trillions of polyethene carry bags are being manufactured and utilized throughout the world. The plastic requires millions of years for natural degradation. The physical and chemical processes are able to degrade plastic material at the meager level by 200 to 500 years in natural conditions. Many industries focus on recycling of plastic. Biodegradation is a comparatively slow and cheaper process that involves microbes. To dispose of plastic completely there is a need of an integrated process in which all the possible methods of disposal are involved and used sustainably so that minimum depletion occurs to the livestock and the environment. In the current review, we could try to emphasize the intricate nature of plastic polymers, pollution caused by it and possible mitigation strategies for plastic waste management. [ABSTRACT FROM AUTHOR]

The conventional heterogeneous photo-Fenton systems suffer from limited surface active sites, sluggish Fe3+/Fe2+ cycle, and low activation efficiency of hydrogen peroxide, thus limiting their applications. Herein a 0D/3D FeOOH/BaTiO3 composite photo-Fenton catalyst system was proposed. The typical microstructure in which FeOOH nanoparticles uniformly anchored on the flower-like BaTiO3 microsphere endows the composite catalysts with abundant active sites and intimate heterojunctions, which are conducive to charge carrier separation and transportation, as confirmed by the electrochemical and XPS characterization results. Benefiting from these advantages, the degradation rate of RhB with 1:4 FeOOH/BaTiO3 was significantly increased to 0.23 min–1, which was 40.5 and 7.9 times higher than that of BaTiO3 and FeOOH when a trace amount of H2O2 (6 mM) was present. In addition, the catalysts also showed superior degradation efficiency in decomposing the antibiotic TC and possessed high recycle stability. The triggered Fenton reactions give rise to abundant •OH, which was confirmed to be the dominated active species. According to the band structure analysis and control experiment results, it was believed the smooth photoelectron transfer from BaTiO3 to FeOOH accelerated the Fe3+/Fe2+ cycle, facilitated activation of H2O2, and boosted photo-Fenton reactions. This work provides a perspective on the design of high-performance photo-Fenton catalysts to tackle wastewater treatment. [ABSTRACT FROM AUTHOR]

Plastics are known for their durability and long decomposition time in the environment, which make plastic recycling an effective approach to mitigate plastic waste risks. However, the global plastic recycling rate is less than 10% mainly due to the labor-intensive and time-consuming nature of the manual recycling process, which poses high health risks and costs. Therefore, the development of a fast, effective, and operational process in current recycling plants is crucial to address the environmental concerns associated with plastics. In the current study, the feasibility of starch/Fe3O4/TiO2 bio-nanocomposite (SFT) as photo-modifiable and photo-degradable was investigated to reduce the workforce in recycling packaging material. The SFT was modified by different UV-C exposure times, which significantly altered its functional properties. The UV-C exposure increased the hydrophobicity of the SFT films and led to a homogenous distribution of Fe3O4/TiO2 nanoparticles (FT). It also increased tensile strength (TS) and decreased elongation at break (EB) of the films. It seems that producing shorter polymer chains, creating new linkages among the polymeric chains, and the homogenous distribution of FT in the matrix of biopolymer by UV-C are the main reasons for these changes. Moreover, the photo-degradation of SFT specimens increased significantly with longer UV-C exposure times. The utilization of magnetic properties in bio-based nanocomposites holds promising potential for streamlining labor-intensive processes in waste recycling plants. However, the inappropriate visual properties of SFT remain a significant obstacle that requires further attention to enable its commercial viability. [ABSTRACT FROM AUTHOR]