Vespa mandarinia (Vespidae: Hymenoptera) is one of the two largest true hornets known to science. The species is a noted predator of social Hymenoptera and a significant pest of managed honey bees in its native range, but is also known to feed on a wide variety of other species when available. Most of the prey records for V. mandarinia are derived from visual observations in Japan, with sparse observations from other parts of its native range. A population of V. mandarinia was detected in North America in 2019 and five nests were removed between 2019 and 2021. We extracted DNA from larval meconia from four nests collected in Washington State, USA, and amplified the CO1 region to determine the potential prey base. We compared these with sequences generated from three nests in the Republic of Korea, and with prey pellets collected from foraging hornets at several locations in Korea. Results indicate that the prey base was much wider in the ROK than the USA, although social Hymenoptera were the most abundant and common prey items in both regions. Prey range seems to be bound by an intersection of organism size and local biodiversity, with little evidence to suggest that the latter is a limiting factor in colony success.

The nanostructured dysprosium oxide ( Dy2O3) was synthesized by the co-precipitation method and incorporated with graphitic carbon nitride (g-C3N4) using the ultrasonication method. The resultant product is denoted as Dy2O3/ g-C3N4 nanocomposite which was further used for electrochemical sensing of riboflavin (RF). The physicochemical properties of Dy2O3/ g-C3N4 nanocomposite were examined using several characterization techniques. The obtained results exhibit the nanocomposite formation with the preferred elemental compositions, functional groups, crystalline phase and desired surface morphology. The electrocatalytic performance of Dy2O3/ g-C3N4 nanocomposite was scrutinized with a glassy carbon electrode (GCE) via differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques with the conventional three-electrode system. The modified electrode distributes more active surface area suggesting high electrocatalytic activity for the RF detection with two linear ranges (0.001–40 μM and 40–150 μM), a low detection limit of 48 nM and sound sensitivity (2.5261 μA μM−1 cm− 2). Further, the designed sensor possesses high selectivity, excellent stability, repeatability and reproducibility. Finally, the fabricated sensor was successfully estimated for the detection of RF in actual food sample analysis using honey and milk with better recovery.

In this research, in order to increase the oxidation resistance of graphite, kaolin and alumina powder with different ratios (26A-74S, 49A-51S, 72A-28S) and slurry method were used to create an aluminosilicate coating on the graphite substrate. In order to reduce the difference in the coefficients of thermal expansion of graphite with aluminosilicate coating, aluminum metaphosphate coating as an interlayer was prepared on the surface of graphite by cathodic electrochemical treatment. The isothermal oxidation test of the samples was carried out in air at a temperature of 1250 °C for 1, 3 and 5 h. The microstructure, chemical composition, and phase components of the coating were, respectively, analyzed by scanning electron microscope equipped with an energy-dispersive spectrometer and X-ray diffraction. The results indicated that, by increasing the withdrawal speed of the samples in slurry method, the amount of changes in the weight of the samples has increased and therefore had a direct effect on oxidation. In addition, it was approved that, at high-temperature oxidation, AlPO4 glass phase forms on aluminum metaphosphate interlayer which retards graphite oxidation. Along with aluminum metaphosphate, aluminosilicate coating also produces a glass phase which fills and seals the voids on the surface which prevents the oxygen to reach the surface of graphite. The created double-layer coating including an interlayer of aluminum metaphosphate + slurry coating prepared with the ratio of 26A-74S as the optimal coating in this research was able to increase the oxidation resistance of graphite by 73% at a temperature of 1250 °C.

The development of heteroatoms doped inorganic nanocrystal-carbon composites (INCCs) has attained a great focus for energy applications (energy production and energy storage). A precise approach to fabricate the INCCs with homogenous distribution of the heteroatoms with an appropriate distribution of metal atoms remains a challenge for material scientists. Herein, we proposed a facile two-step route to synthesize INCC with doping of metal (α-Fe2O3) and non-metals (N, P, O) using hydrogel formed by treating hexachlorocyclotriphosphazene (HCCP) and 3, 4, 5-trihydroxy benzoic acid (Gallic acid). Metal oxide was doped using an extrinsic doping approach by varying its content and non-metallic doping by an intrinsic doping approach. We have fabricated four different samples (INCC-0.5%, INCC-1.0%, INCC-1.5%, and INCC-2.0%), which exhibit the uniform distribution of the N, P, O, and α-Fe2O3 in the carbon architecture. These composite materials were applied as anode material in water oxidation catalysis (WOC); INCC-1.5% electro-catalyst confirmed by cyclic voltammetry (CV) with a noticeable catholic peak 0.85 V vs RHE and maximal current density 1.5 mA.cm−2. It also delivers better methanol tolerance and elongated stability than RuO2; this superior performance was attributed due to the homogenous distribution of the α-Fe2O3 causing in promotion of adsorption of O2 initially and a greater surface area of 1352.8 m2/ g with hierarchical pore size distribution resulting higher rate of ion transportation and mass-flux.

The ability to both assay the presence of, and to selectively remove ions in a solution is an important tool for waste water treatment in many industrial sectors, especially the nuclear industry. Nuclear waste streams contain high concentrations of heavy metals ions and radionuclides, which are extremely toxic and harmful to the environment, wildlife and humans. For the UK nuclear industry alone, it is estimated that there will be 4.9 million metric tonnes of radioactive waste by 2125, which contains a significant number of toxic radionuclides and heavy metals. This is exacerbated further by increased international growth of nuclear new build and decommissioning. Efforts to remove radionuclides have been focused on the development and optimisation of current separation and sequestering techniques as well as new technologies. Due to the large volumes of waste the techniques must be economical, simple to use and highly efficient in application. Magnetic nanoparticles (MNPs) offer a powerful enhancement of normal ion exchange materials in that they can be navigated to specific places using external magnetic fields and hence can be used to investigate challenges such as, pipework in preparation of decommissioning projects. They also have the potential to be fine-tuned to extract a variety of other radionuclides and toxic heavy metals. It has been demonstrated that with the right functional groups these particles become very strongly selective to radionuclides, such as Uranium. However, this new technology also has the potential to effectively aid nuclear waste remediation at a low cost for the separation of both radionuclides and heavy metals. In this work, we investigate the origin of the selectivity of superparamagnetic iron oxide nanoparticles (SPIONs) to Uranium by making systematic changes to the existing surface chemistry and determining how these changes influence the selectivity. Identifying the mechanism by which selected common nuclear related metals, such as Na(I), K(I), Cs(I), Ca(II), Cu(II), Co(II), Ni(II), Cd(II), Mg(II), Sr(II), Pb(II), Al(III), Mn(II), Eu(III) and Fe(III), are sorbed will allow for specific NP-target (nanoparticle) ion interactions to be revealed. Ultimately this understanding will provide guidance in the design of new targeted NP-ligand constructs for other environmental systems.

Echeveria is a genus belonging to the Crassulaceae family that comprises approximately 170 species. It is a representative plant known as a succulent with economic potential in the floriculture industry. Echeveria plants are widely distributed in dry environments and endemic to Mexico. These plants have a rosette formation and varied leaf colors and shapes, which are characteristics of interest for landscaping, cut flowers, or interior decoration. Given their range of locations in different climates or indoor conditions, it is important to have an understanding and knowledge of their leaf morphology and anatomy and how they function to provide optimum care and management. Owing to high demand in horticultural markets, many breeders have crossed their desired species. However, this method has progressively increased the number of species without proper records of parents or other natural unintended crossings, creating phylogenetic problems and identification issues. The use and understanding of phenotypes, anatomical data, and/or research to aid in taxonomic issues and improve cultural management practices have been reviewed and discussed in this paper. In this review, we have provided a brief background of Echeveria species, focusing on the challenges and studies that have attempted to address these issues.

The surface of carbon films deposited with inverted plasma fireballs is analysed in this paper. Measurements were conducted with Raman spectroscopy, atomic force microscopy and nanoindentation. The latter was used to obtain Young’s modulus as well as Martens and Vickers hardness. The roughness of the film was measured by atomic force microscopy and its thickness was measured. It was shown with Raman spectroscopy that the films are homogeneous in terms of atomic composition and layer thickness over an area of about 125 × 125 mm. Furthermore, it was demonstrated that inverted plasma fireballs are a viable tool for obtaining homogeneous, large area carbon films with rapid growth and very little energy consumption. The obtained films show very low roughness.

There is an ever growing interest in the development of biochar from a large variety of agrowastes. Herein, the main objective is the conversion of pomegranate peel powder biochar and its post-functionalization by phosphoric acid treatment, followed by arylation organic reaction. The latter was conducted using in situ-generated diazonium salts of 4-aminobenzoic acid ( H2N-C6H4-COOH), sulfanilic acid ( H2N-C6H4-SO3H) and Azure A dye. The effect of diazonium nature and concentration on the arylation process was monitored using thermal gravimetric analysis (TGA) and Raman spectroscopy, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). SEM pictures showed micrometer-sized biochar particles with tubular structure having about 10–20 μm-wide channels. SEM studies have shown that arylation did not affect the morphology upon arylation. The porous structure did not collapse and withstood the arylation organic reaction in acid medium did not collapse upon arylation. TGA and Raman indicated gradual changes in the arylation of biochar at initial concentrations 10– 5, 10– 4 and 10– 3 mol L− 1 of 4-aminobenzoic acid. The detailed Raman spectra peak fittings indicate that the D/G peak intensity ratio leveled off at 3.35 for 4-aminobenzoic acid initial concentration of 10– 4 mol L− 1, and no more change was observed, even at higher aryl group mass loading. This is in line with formation of oligoaryl grafts rather than the grafting of new aryl groups directly to the biochar surface. Interestingly, Azure A diazonium salt induced much lower extent of surface modification, likely due to steric hindrance. To the very best of our knowledge, this is the first report on diazonium modification of agrowaste-derived biochar and opens new avenues for arylated biochar and its applications.

Molten salt consisting primarily of eutectic LiCl-KCl is currently being used in electrorefiners in the Fuel Conditioning Facility at Idaho National Laboratory. Options are currently being evaluated for storing this salt outside of the argon atmosphere hot cell. The hygroscopic nature of eutectic LiCl-KCl makes is susceptible to deliquescence in air followed by extreme corrosion of metallic cannisters. In this study, the effect of occluding the salt into a zeolite on water sorption/desorption was tested. Two zeolites were investigated: Na-Y and zeolite 4A. Na-Y was ineffective at occluding a high percentage of the salt at either 10 or 20wt% loading. Zeolite-4A was effective at occluding the salt with high efficiency at both loading levels. Weight gain in salt occluded zeolite-4A (SOZ) from water sorption at 20% relative humidity and 40℃ was 17wt% for 10% SOZ and 10wt% for 20% SOZ. In both cases, neither deliquescence nor corrosion occurred over a period of 31 days. After hydration, most of the water could be driven off by heating the hydrated salt occluded zeolite to 530℃. However, some HCl forms during dehydration due to salt hydrolysis. Over a wide range of temperatures (320–700℃) and ramp rates (5, 10, and 20℃ min−1), HCl formation was no more than 0.6% of the Cl− in the original salt.

Carbon fibers are commonly used in many specialized, high-performance applications such as race cars and aircraft due to their lightweight and high durability. The most important stage in the production of carbon fibers is the carbonization process. During this process, carbon fibers are subjected to high temperatures in the absence of oxygen to prevent fibers from burning. Labyrinth seals are attached to a carbonization furnace to prevent airflow into the furnace and to assist in the elimination of off-gases. This study investigated flow characteristics inside a carbonization furnace and the effects of different geometric parameters of labyrinth seals such as labyrinth tooth shape, number of teeth, and tooth clearance. Varying carbonization furnace operating conditions were also studied in regard to flow behavior, including fiber movement and outlet vacuum pressure. A high working gas flow rate at the furnace inlet resulted in recirculation zones. Properly regulated gas flow from the main and labyrinth inlets enabled uniform flow around the fibers’ inlet and outlet which prevented air from being trapped in the reactor. Flow behavior was minimally effected by changes to labyrinth seal geometry such as tooth length, tooth clearance, and outlet pressure. However, the movement of fibers had a clear effect on flow characteristics in the furnace.

Fluorescent nanostructures based on carbon, or carbon dots, are attracting much attention and interest because of their diverse properties which can be applied in several fields of knowledge, such as optics, biomedicine, environmental research, among others. Such properties are in part, derived from its intrinsic luminescence from tunable functional groups. In this work, we produced carbon nanodots (CND) using agro-industrial residues, such as Lolium perenne and malt bagasse. The methods used were conventional hydrothermal syntheses and microwave-assisted hydrothermal synthesis. To the best of our knowledge, this is the first time that carbon dots synthesized from this ryegrass type are reported. The synthesis methods were one step (no catalyst, base, or acid were added for passivation), and the functional groups responsible for the luminescence and high solubility in water were identified by infrared spectroscopy, being mainly C=O, C–OH, C–N, and N–H. According to our theoretical studies, the C=O group introduced a new energy level for electronic transitions that can affect the emission properties. Fluorescence images of osteoblasts using CNDs were acquired and their chelating property towards Pb2+ and Cr6+ detection was tested.

The carbon-based nanostructures are in limelight due to their widespread applications in nano-to-micro-scale technologies. The carbon dots are known for their unique physical, electrical, optical, chemical and biological properties. The carbon dots (CDs) are being produced through several well-developed synthesis methods, one of which is the green sonochemical. This method is preferred over others because it is a green source of energy, facile, fast, low-temperature process, non-toxic and less expensive. Despite the fact of using 90% less energy than other methods, this method has been overlooked in the published literature. It is possible to prepare pure and doped CDs of low toxicity and controlled physicochemical properties through sonochemical method. In recent years, sonochemically produced CDs have been tuned and characterized for a variety of applications. This review has explored the merits and demerits of sonochemical method in comparison to the other methods for the synthesis of pure CDs and their nanocomposites. The role of multiple factors in tailoring the specific parameters of CDs for their application in antibacterial, polymerization, tissue engineering, catalysis, bio-imagining, supercapacitors, drug delivery and electric devices is also elaborated in this review. This review also concludes on future directions in the applications of sonochemically produced CDs.

Activated non-graphitizable hard carbon using orange peel with mesoporous structure has been prepared by pyrolyzation at 700, 800, 900 °C using chemical activation method. The activated orange peel-derived hard carbon has been characterized for its mesoporous and disordered structure. TG-DSC gives the information for the changes about sample composition and thermal stability of the materials. Increasing the carbonization temperature for orange peel precursor using NaOH as activating agent, elevates the pore diameter, which thereby facilitating the insertion of Na+. Raman and X-ray diffraction confirms the presence of disordered carbon. The surface morphology of the material was analyzed by scanning eletron microsope and nitrogen ( N2) adsorption and desorption analysis give the morphology, mesopore size (3.374, 3.39 and 4 nm) and surace area (60.164, 58.99 and 54.327 m2/g) of the orange peel-derived hard carbon. Hence, this work strongly evidences that the biomass-derived hard carbon with good porosity and paves way of superior electrochemical performance for emerging sodium ion batteries.

Most recently, graphene-related composite-modified electrode surfaces are been widely employed to improve surface interactions and electron transfer kinetics. Hydrothermally prepared strontium pyro niobate (SPN) and reduced graphene oxide/ strontium pyro niobate (RGOSPN) nanostructures reveal excellent morphology. X-ray diffraction analysis of SPN and RGOSPN agree with standard data. Thermogravimetry–differential scanning calorimetry analyses show that RGOSPN has higher thermal stability than SPN. In addition, from the polarization–electric field (P–E) loop measurements, the estimated value of remnant polarization (Pr) and coercive electric field (Ec) of SPN are 0.039 μC cm−2 and − 2.90 kV cm−1 and that of RGOSPN nanocomposite are 0.0139 μC cm−2 and − 2.04 kV cm−1. Cyclic voltammetry measurements show that RGOSPN nanocomposite manifests the possibility of electrochemical reversibility beyond long cycles without change in performance. The redox cycle reveal that RGOSPN can be used as part of a composite electrode for hybrid capacitors dynamic conditions. Moreover, the specific capacitance of SPN and RGOSPN was calculated using galvanostatic charge–discharge (GCD) technique. The observed energy density of 9.1 W h kg−1 in RGOSPN is higher when compared with previous reported values.

This work reports the syntheses of an inexpensive and efficient asphalt-derived mesoporous carbon (AdMC) as an adsorbent. The adsorbent was activated with potassium hydroxide to increase its surface area and then characterized by SEM–EDS, FT-IR, and BET. The adsorption properties of AdMC were evaluated for the adsorptive removal of eleven Poly Aromatic Hydrocarbons (PAHs) and diesel from water samples. The prepared AdMC showed very high surface areas and high micropore volumes equal to 2316 m2/g and 1.2 cm3/g, respectively. Various experimental conditions influencing the adsorption capacity of eleven PAHs and diesel were investigated. At high concentrations, PAHs and diesel solubility in water is very low. Hence, samples were emulsified with a surfactant, and then maximum adsorption capacity was investigated. Adsorption profile of individual PAHs was examined using gas chromatography/mass spectrometry analysis followed by liquid–liquid extraction. Total hydrocarbon removal was studied using a total organic analyzer. Asphalt-derived mesoporous sorbent showed an extreme ability to remove PAHs and diesel (average adsorption capacity of 166 mg/g for individual PAHs and diesel (maximum capacity of 1600 mg/g). The experimental results fitted the Langmuir model with a correlation efficiency of 0.9853. The results obtained for both adsorbents also matched to pseudo-second-order kinetics, suggesting that the adsorption of PAHs and diesel is chemical, monolayer, and homogeneous process.

Objectives: This systematic review examined the association of animal-assisted interventions (AAI) with quality of life (QoL) for pediatric oncology patients, for potential use in occupational therapy practice. Methods: Articles published in peer-reviewed journals between 2002-2019 from PubMed, MEDLINE, CINAHL, American Journal of Occupational Therapy (AJOT), Journal of Oncology, SCOPUS, and OTSeeker were selected for AAI with therapy dogs specific to the target population of pediatric oncology patients undergoing treatment in clinical settings. Results: Moderate evidence was found for AAI and mood improvement, pain reduction, and stress relief; and low-level evidence supported AAI for decreasing anxiety. The most significant AAI improvements were seen in perceptions of pain, stress levels, and mood. Discussion: Evidence suggests that occupational therapists may want to consider incorporating AAI into therapy sessions as it serves as a distraction and short-term coping strategy for children undergoing oncological treatment.