Currindall7627

5 mL of DA (SNP-1.5DA) showed a better adsorption performance compared to the samples prepared with 0.5 and 1.0 mL of DA (SNP-0.5DA and SNP-1.0DA, respectively). The main factor affecting the adsorption efficiency was found to be the available surface area for each nanocomposite, which was directly related to the degree of crystallinity as obtained by XRD analysis.Developing efficient catalysts to produce clean fuel by using solar energy has long been the goal to mitigate the issue of traditional fossil fuel scarcity. In this work, we design a heterostructure photocatalyst by employing two green components, Ni(OH)2 and ZnIn2S4, for efficient photocatalytic H2 evolution under the illumination of visible light. After optimization, the obtained photocatalyst exhibits an H2 evolution rate at 0.52 mL h-1 (5 mg) (i.e., 4640 μmol h-1 g-1) under visible light illumination. Further investigations reveal that such superior activity is originated from the efficient charge separation due to the two-dimensional (2D) structure of ZnIn2S4 and existing high-quality heterojunction.Many efforts have recently concentrated on constructing and developing nanoparticles (NPs) as promising thermal agent for optical hyperthermia and photothermal therapy. However, thermal energy transfer in biological tissue is a complex process involving different mechanisms such as conduction, convection, radiation. Therefore, having information about thermal properties of tissue especially when NPs are embedded in is a necessity for predicting the heat transfer during hyperthermia. In this work, the thermal properties of solid phantom based on agar in the presence of three different nanoparticles (BPSi, tNAs, GNRs) and alone were measured and reported as a function of temperature (ranging from 22 to 62 °C). The thermal response of these NPs to an 808 nm laser beam with three different powers were studied in the water comparatively. Agar and tNAs have almost constant thermal properties in the considered range. Among the three NPs, gold has the highest conductivity and diffusivity. At 62 °C BPSi NPs have the similar amount of increase for the diffusivity. The thermal parameters reported in this paper can be useful for the mathematical modeling. Irradiation of the NPs-loaded water phantom displayed the highest radiosensitivity of gold among the three mentioned NPs. However, for the higher power of irradiation, BPSi and tNAs NPs showed the increased absorption of heat during shorter time and the increased temperature gradient slope for the initial 15 s after the irradiation started. The three NPs showed different thermal and irradiation response behavior; however, this comparison study notes the worth of having information about thermal parameters of NPs-loaded tissue for pre-clinical planning.In this study, the influence of graphene oxide nanoparticles on the bond-slip behavior of fiber and fly-ash-based geopolymer paste was examined. Geopolymer paste incorporating a graphene oxide nanoparticle solution was cast in half briquetted specimens and embedded with a fiber. Three types of fiber were used steel, polypropylene, and basalt. The pullout test was performed at two distinct speeds 1 mm/s and 3 mm/s. The results showed that the addition of graphene oxide increased the compressive strength of the geopolymer by about 7%. The bond-slip responses of fibers embedded in the geopolymer mixed with graphene oxide exhibited higher peak stress and toughness compared to those embedded in a normal geopolymer. Each fiber type also showed a different mode of failure. Both steel and polypropylene fibers showed full bond-slip responses due to their high ductility. Basalt fiber, on the other hand, because of its brittleness, failed by fiber fracture mode and showed no slip in pullout responses. PLX-4720 Both bond strength and toughness were found to be rate-sensitive. The sensitivity was higher in the graphene oxide/geopolymer than in the conventional geopolymer.Metal effects on the gas sensing behavior of metal complexes of 5,10,15,20-tetrakis(4-hydroxyphenyl)porphyrin (THPP) thin film was investigated in terms of detecting NO2 gas by the planar optical waveguide. For this purpose, several THPP and metal complexes were synthesized with different central metal ions Co(II), Ni(II), Cu(II), and Zn(II). Planar optical gas sensors were fabricated with the metalloporphyrins deposited on K+ ion-exchanged soda-lime glass substrate with the spin coating method serving as host matrices for gas interaction. All of the THPP complex's films were fully characterized by UV-Vis, IR and XPS spectroscopy, and the laser light source wavelength was selected at 520 and 670 nm. The results of the planar optical waveguide sensor show that the Zn-THPP complex exhibits the strongest response with the lowest detectable gas concentration of NO2 gas for both 520 nm and 670 nm. The Ni-THPP and Co-THPP complexes display good efficiency in the detection of NO2, while, on the other hand, Cu-THPP shows a very low interaction with NO2 gas, with only 50 ppm and 200 ppm detectable gas concentration for 520 nm and 670 nm, respectively. In addition, molecular dynamic simulations and quantum mechanical calculations were performed, proving to be coherent with the experimental results.We report the successful synthesis and a complete magnetic characterization of CoFe2O4@SiO2@Au magnetoplasmonic nanoparticles. The CoFe2O4 magnetic nanoparticles were prepared using the hydrothermal method. A subsequent SiO2 shell followed by a plasmonic Au shell were deposited on the magnetic core creating magnetoplasmonic nanoparticles with a core-shell architecture. A spin-glass-type magnetism was shown at the surface of the CoFe2O4 nanograins. Depending on the external magnetic field, two types of spin-glass were identified and analyzed in correlation with the exchange field acting on octahedral and tetrahedral iron sites. The magnetization per formula unit of the CoFe2O4 core is not changed in the case of CoFe2O4@SiO2@Au nanocomposites. The gold nanoparticles creating the plasmonic shell show a giant diamagnetic susceptibility, dependent on their crystallite sizes.The occurrence of nanoplastics (NPs) and microplastics (MPs) in aquatic ecosystems and their capacity to sorb hydrophobic pollutants is nowadays an issue of great concern. This study aimed to assess the potential bioavailability and acute toxicity of polystyrene (PS) NPs (50 and 500 nm) and of MPs (4.5 µm), alone and with sorbed benzo(a)pyrene (B(a)P), in the embryo/larval stages of brine shrimps and zebrafish. Exposure to pristine plastics up to 50.1 mg PS/L did not cause significant impact on brine shrimp survival, while some treatments of plastics-B(a)P and all concentrations of B(a)P (0.1-10 mg/L) resulted acutely toxic. In zebrafish, only the highest concentrations of MPs-B(a)P and B(a)P caused a significant increase of malformation prevalence. Ingestion of NPs was observed by 24-48 h of exposure in the two organisms (from 0.069 to 6.87 mg PS/L). In brine shrimps, NPs were observed over the body surface and within the digestive tract, associated with feces. In zebrafish, NPs were localized in the eyes, yolk sac, and tail at 72 h, showing their capacity to translocate and spread into the embryo. MP ingestion was only demonstrated for brine shrimps. In zebrafish embryos exposed to plastics-B(a)P, B(a)P appeared in the yolk sac of the embryos. The presence of B(a)P was also noticeable in brine shrimps exposed to 500 nm NPs-B(a)P. In conclusion, NPs entered and spread into the zebrafish embryo and PS NPs, and MPs were successful vectors of B(a)P to brine shrimp and zebrafish embryos. Particle size played a significant role in explaining the toxicity of plastics-B(a)P. Our study provides support for the idea that plastics may pose a risk to aquatic organisms when combined with persistent organic pollutants such as B(a)P.The rapidly advancing technology of wearable and miniaturized electronics has increased the demand for low-cost high-performance flexible sensors. Herein, the preparation of translucent freestanding films consisting of cellulose nanofibers (CNFs) and ZnO nanoparticles (NPs) via a simple spray coating method is presented. The obtained nanocomposite films were thin (~10 µm) and flexible. The scanning electron microscopy and atomic force microscopy analysis revealed that the nanocomposite film was composed of regions of ZnO NP-modified CNFs and regions of aggregation of ZnO NPs with each other. The electrical conductance of the films was rapidly increased beyond 40 wt.% ZnO and reached up to >50 nA at 60 wt.% ZnO. This was attributed to the increased number of conductive paths formed by the ZnO NPs in the nanocomposite film when a certain threshold was crossed. The ZnO-CNF nanocomposite film exhibited a stable response over on/off cycles of UV light exposure. The responsivity and sensitivity of the nanocomposite film with 60 wt.% ZnO were 36.5 mA/W and 247, respectively. Even when the device was curved (radius of curvature 3 mm), the response and sensitivity remained high. The developed nanocomposite films are expected to be applied as environmentally friendly flexible UV sensors.Herein, we report high electrocatalytic activity of monoclinic VO2 (M1 phase) for the oxygen evolution reaction (OER) for the first time. The single-phase VO2 (M1) nanoparticles are prepared in the form of uniformly covering the surface of individual carbon fibers constituting a carbon fiber paper (CFP). The VO2 nanoparticles reveal the metal-insulator phase transition at ca. 65 °C (heating) and 62 °C (cooling) with low thermal hysteresis, indicating a high concentration of structural defect which is considered a grain boundary among VO2 nanoparticles with some particle coalescence. Consequently, the VO2/CFP shows a high electrocatalytic OER activity with the lowest η10 (350 mV) and Tafel slope (46 mV/dec) values in a 1 M aqueous solution of KOH as compared to those of the vacuum annealed V2O5 and the hydrothermally grown VO2 (M1), α-V2O5, and γ'-V2O5. The catalytically active site is considered V4+ components and V4+/5+ redox couples in VO2. The oxidation state of V4+ is revealed to be more favorable to the OER catalysis compared to that of V5+ in vanadium oxide through comparative studies. Furthermore, the amount of V5+ component is found to be increased on the surface of VO2 catalyst during the OER, giving rise to the performance degradation. This work suggests V4+ and its redox couple as a novel active component for the OER in metal-oxide electrocatalysts.A randomly oriented nanowire network, also called nanonet (NN), is a nano-microstructure that is easily integrated into devices while retaining the advantages of using nanowires. This combination presents a highly developed surface, which is promising for sensing applications while drastically reducing integration costs compared to single nanowire integration. It now remains to demonstrate its effective sensing in real conditions, its selectivity and its real advantages. With this work, we studied the feasibility of gaseous acetone detection in breath by considering the effect of external parameters, such as humidity and temperature, on the device's sensitivity. Here the devices were made of ZnO NNs covered by SnO2 and integrated on top of microhotplates for the fine and quick control of sensing temperature with low energy consumption. The prime result is that, after a maturation period of about 15 h, the devices are sensitive to acetone concentration as low as 2 ppm of acetone at 370 °C in an alternating dry and wet (50% of relative humidity) atmosphere, even after 90 h of experiments.