Optimization of Sandwich Composites Fuselages Under Flight Loads

The sandwich composites fuselages appear to be a promising choice for the future aircrafts because of their structural efficiency and functional integration advantages. However, the design of sandwich composites is more complex than other structures because of many involved variables. In this paper, the fuselage is designed as a sandwich composites cylinder, and its structural optimization using the finite element method (FEM) is outlined to obtain the minimum weight. The constraints include structural stability and the composites failure criteria. In order to get a verification baseline for the FEM analysis, the stability of sandwich structures is studied and the optimal design is performed based on the analytical formulae. Then, the predicted buckling loads and the optimization results obtained from a FEM model are compared with that from the analytical formulas, and a good agreement is achieved. A detailed parametric optimal design for the sandwich composites cylinder is conducted. The optimization method used here includes two steps: the minimization of the layer thickness followed by tailoring of the fiber orientation. The factors comprise layer number, fiber orientation, core thickness, frame dimension and spacing. Results show that the two-step optimization is an effective method for the sandwich composites and the foam sandwich cylinder with core thickness of 5 mm and frame pitch of 0.5 m exhibits the minimum weight.     

Towards carbon-free flame spray synthesis of homogeneous oxide nanoparticles from aqueous solutions

Flame-assisted spray pyrolysis (FASP) is a versatile process for synthesis of nanoparticles from a broad choice of precursors and solvents. Water is an attractive solvent particularly for inexpensive inorganic precursors (e.g. metal nitrates) as it can effectively reduce the process cost. Furthermore when water usage is combined with a carbon-free fuel (e.g. H₂), nanoparticles can be made without forming CO₂. Here such a FASP process is explored for synthesis of Bi₂O₃ and other oxide nanoparticles from aqueous precursor solutions. The flame temperature was measured by FTIR emission–transmission spectroscopy while powders were characterized by X-ray diffraction and N₂ adsorption. At low FASP fuel gas (H₂ or C₂H₂) flow rates or process temperatures, product powders had a bimodal crystal size distribution. Its large and small modes were made by droplet- and gas-to-particle conversion, respectively. Homogeneous Bi₂O₃ and CeO₂ powders were obtained for sufficiently high flow rates of either C₂H₂ or H₂. Prolonged high temperature residence times promoted precursor evaporation from the spray droplets and yielded homogeneous nanostructured powders by gas-to-particle conversion. In contrast, FASP of aqueous solutions of aluminum nitrate yielded rather large particles by droplet-to-particle conversion at all fuel flows investigated.     

Toxicity of Silver Nanoparticles in Macrophages

Silver nanoparticles (nanosilver) are broadly used today in textiles, food packaging, household devices and bioapplications, prompting a better understanding of their toxicity and biological interactions. In particular, the cytotoxicity of nanosilver with respect to mammalian cells remains unclear, because such investigations can be biased by the nanosilver coatings and the lack of particle size control. Here, nanosilver of well‐defined size (5.7 to 20.4 nm) supported on inert nanostructured silica is produced using flame aerosol technology. The cytotoxicity of the prepared nanosilver with respect to murine macrophages is assessed in vitro because these cells are among the first to confront nanosilver upon its intake by mammals. The silica support facilitates the dispersion and stabilization of the prepared nanosilver in biological suspensions, and no other coating or functionalization is applied that could interfere with the biointeractions of nanosilver. Detailed characterization of the particles by X‐ray diffraction and electron microscopy reveals that the size of the nanosilver is well controlled. Smaller nanosilver particles release or leach larger fractions of their mass as Ag⁺ ions upon dispersion in water. This strongly influences the cytotoxicity of the nanosilver when incubated with murine macrophages. The size of the nanosilver dictates its mode of cytotoxicity (Ag⁺ ion‐specific and/or particle‐specific). The toxicity of small nanosilver (<10 nm) is mostly mediated by the released Ag⁺ ions. The influence of such ions on the toxicity of nanosilver decreases with increasing nanosilver size (>10 nm). Direct silver nanoparticle–macrophage interactions dominate the nanosilver toxicity at sizes larger than 10 nm.     

Challenges and opportunities in renovating public sector information by enabling linked data and analytics

Linked Data has become the current W3C recommended approach for publishing data on the World Wide Web as it is sharable, extensible, and easily re-usable. An ecosystem of linked data hubs in the Public Sector has the potential to offer significant benefits to its consumers (other public offices and ministries, as well as researchers, citizens and SMEs), such as increased accessibility and re-use value of their data through the use of web-scale identifiers and easy interlinking with datasets of other public data providers. The power and flexibility of the schema-defying Linked Data, however, is counterbalanced by inborn factors that diminish the potential for cost-effective and efficient adoption by the Public Sector. The paper analyzes these challenges in view of the current state-of-the-art in linked data technologies and proposes a technical framework that aims to hide the underlying complexity of linked data while maintaining and promoting the interlinking capabilities enabled by the Linked Data Paradigm. The paper presents the innovations behind our proposed solutions as well as their advantages, especially for the non-expert users.     

Characteristics and Catalytic Properties of Pd/SiO2 Synthesized by One-step Flame Spray Pyrolysis in Liquid-phase Hydrogenation of 1-Heptyne

In this study, Pd/SiO₂ catalysts with 0.5–10 wt.% Pd loadings were prepared by one-step flame spray pyrolysis (FSP) and characterized by N₂ physisorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), CO chemisorption, and X-ray photoelectron spectroscopy (XPS). The average cluster/particles size of Pd as revealed by TEM were ca. 0.5–3 nm. The turnover frequencies (TOFs) of the flame-made catalysts decreased from 66.2 to 4.3 per s as Pd loading increased from 0.5 to 10 wt.%, suggesting that the catalytic activity was dependent on Pd particle/cluster size. However, there were no appreciable influences on 1-heptene selectivity. The flame-made Pd/SiO₂ showed better properties than the conventional prepared catalysts. Their advantages are not only the presence of large pores that facilitates diffusion of the reactants and products, but also the high-catalytic activity of as-synthesized catalysts so that further pretreatment is not necessary.     

Thermodynamics of Vapor Synthesis of AlN by Nitridation of Aluminum and Its Halides

A thermodynamic analysis for the vapor synthesis of AlN is presented. A thermodynamic equilibrium computer code and recent thermochemical tables are used to evaluate various reactant gases for their potential to produce high-purity AlN at high yields. The Al/N/H/X/Y systems are examined, where X is any halide atom and Y is an inert gas. The effects of reactant ratio, temperature, and pressure on reactant conversion and product purity are estimated. Results from two systems are presented in the form of design diagrams, which represent the phases formed and the conversion achieved at various process conditions.     

Continuous flame aerosol synthesis of carbon-coated nano-LiFePO4 for Li-ion batteries

Core–shell, nano-sized LiFePO₄-carbon particles were made in one step by scalable flame aerosol technology at 7 g/h. Core LiFePO₄ particles were made in an enclosed flame spray pyrolysis (FSP) unit and were coated in-situ downstream by auto thermal carbonization (pyrolysis) of swirl-fed C₂H₂ in an O₂-controlled atmosphere. The formation of acetylene carbon black (ACB) shell was investigated as a function of the process fuel-oxidant equivalence ratio (EQR). The core–shell morphology was obtained at slightly fuel-rich conditions (1.0<EQR<1.07) whereas segregated ACB and LiFePO₄ particles were formed at fuel-lean conditions (0.8<EQR<1). Post-annealing of core–shell particles in reducing environment (5 vol% H₂ in argon) at 700 °C for up to 4 h established phase pure, monocrystalline LiFePO₄ with a crystal size of 65 nm and 30 wt% ACB content. Uncoated LiFePO₄ or segregated LiFePO₄–ACB grew to 250 nm at these conditions. Annealing at 800 °C induced carbothermal reduction of LiFePO₄ to Fe₂P by ACB shell consumption that resulted in cavities between carbon shell and core LiFePO₄ and even slight LiFePO₄ crystal growth but better electrochemical performance. The present carbon-coated LiFePO₄ showed superior cycle stability and higher rate capability than the benchmark, commercially available LiFePO₄.     

Silver Nanoparticles from Oregano Leaves’ Extracts as Antimicrobial Components for Non-Infected Hydrogel Contact Lenses

The oregano leaves’ extract (ORLE) was used for the formation of silver nanoparticles (AgNPs(ORLE)). ORLE and AgNPs(ORLE) (2 mg/mL) were dispersed in polymer hydrogels to give the pHEMA@ORLE_2 and pHEMA@AgNPs(ORLE)_2 using hydroxyethyl–methacrylate (HEMA). The materials were characterized by X-ray fluorescence (XRF) spectroscopy, X-ray powder diffraction analysis (XRPD), thermogravimetric differential thermal analysis (TG-DTA), derivative thermogravimetry/differential scanning calorimetry (DTG/DSC), ultraviolet (UV-Vis), and attenuated total reflection mode (ATR-FTIR) spectroscopies in solid state and UV–Vis in solution. The crystallite size value, analyzed with XRPD, was determined at 20 nm. The antimicrobial activity of the materials was investigated against Gram-negative bacterial strains Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli). The Gram-positive ones of the genus of Staphylococcus epidermidis (S. epidermidis) and Staphylococcus aureus (S. aureus) are known to be involved in microbial keratitis by the means of inhibitory zone (IZ), minimum inhibitory concentration (MIC), and minimum bactericidal concentration (MBC). The IZs, which developed upon incubation of P. aeruginosa, E. coli, S. epidermidis, and S. aureus with paper discs soaked in 2 mg/mL of AgNPs(ORLE), were 11.7 ± 0.7, 13.5 ± 1.9, 12.7 ± 1.7, and 14.3 ± 1.7 mm. When the same dose of ORLE was administrated, the IZs were 10.2 ± 0.7, 9.2 ± 0.5, 9.0 ± 0.0, and 9.0 ± 0.0 mm. The percent of bacterial viability when they were incubated over the polymeric hydrogel discs of pHEMA@AgNPs(ORLE)_2 was interestingly low (66.5, 88.3, 77.7, and 59.6%, respectively, against of P. aeruginosa, E. coli, S. epidermidis, and S. aureus) and those of pHEMA@ORLE_2 were 89.3, 88.1, 92.8, and 84.6%, respectively. Consequently, pHEMA@AgNPs(ORLE)_2 could be an efficient candidate toward the development of non-infectious contact lenses.     

Optimal Doping for Enhanced SnO2 Sensitivity and Thermal Stability

Tin oxide nanocrystals (5–10 nm) doped with silica (0–15 wt %) were made by flame‐spray‐pyrolysis direct deposition onto the sensing electrodes and in situ stabilization by rapid flame annealing. Although increased SiO₂‐doping reduced the SnO₂ crystal and grain size, its sensing performance to ethanol vapor (0.1–50 ppm) exhibited an optimum with respect to SiO₂ content. The thermal stability and morphology of SiO₂‐doped SnO₂ nanoparticles were evaluated by sintering at 200–900 °C for 4–24 h in air. At low SiO₂ content, sintering of SnO₂ was prevented only partially resulting in small sinter necks (bottlenecks) between SnO₂ primary particles (smaller than twice the Debye length). This morphology drastically enhanced the sensitivity toward the analyte by maintaining a thermally stable high surface area and fully depleted connections at the primary particle necks. This enhancement is attributed mostly to the decreasing neck size of the SnO₂ SiO₂ heterojunctions rather than the decreasing SnO₂ crystallite and grain sizes with increasing SiO₂ doping. At high SiO₂ contents, SnO₂ sintering was inhibited as its grains were separated effectively by dielectric SiO₂; this resulted in isolated SnO₂ nanocrystals with drastically reduced sensitivity, thereby effectively being insulators.