Improved electrical conductivity of a non-covalently dispersed graphene–carbon nanotube film by chemical p-type doping

Using a high-pressure air spray we developed a method to deposit electrically-conducting thin films consisting of non-covalently dispersed graphene and carbon nanotubes. The graphene–carbon nanotube film was immersed in a nitric acid and followed by exposure to fuming nitric acid. The acid treatment induced an increased concentration of atomic nitrogen on the graphene basal plane and carbon nanotube sidewall. This result indicates chemical p-type doping of the graphene oxide–carbon nanotube film. After the two acid treatments, the spray coated graphene oxide–carbon nanotube films on a glass substrate exhibit a low sheet resistance of 171 Ω/sq, and a high transmittance of 84% at a wavelength of 550 nm.     

Physical and potentiometric properties of polyurethane‐based cation‐selective membranes

Lipophilic salts based on tetraphenylborate derivatives [e.g., potassium tetrakis(p‐chlorophenyl)borate (KTpClPB), sodium tetraphenylborate (NaTPB), and cesium tetrakis(3‐methylphenyl)borate are essential ingredients used in the preparation of solvent polymeric cation‐selective membranes. The effects of such lipophilic salts on the physical properties of a polyurethane (PU) matrix comprising 4,4′‐diphenylmethane diisocyanate, 1,4‐butanediol, and poly(tetramethylene ether glycol) were examined. Differential scanning calorimetry measurements revealed that the sodium and potassium salts doped in PU increased the glass‐transition temperatures (T_g) of the matrix, while the film containing cesium salt exhibited slightly decreased T_g. The temperature dependence of the ionic conductivity for PU60 films doped with KTpClPB is well described by the Arrhenius‐type equation, and that doped with NaTPB is described by the Vogel–Tammann–Fulcher (VTF)‐type equation. The temperature dependence of the ionic conductivity on the VTF‐type equation suggests that the transport of sodium ions in the PU60 matrix is more strongly coupled to the soft segmental motion, and potassium ions are decoupled from the polymer host and transported by activated hopping. The effect of added salt on the internal structure of PU membranes was investigated by measuring the ratio between the free and hydrogen‐bonded CO bands at 1703 and 1730 cm⁻¹, respectively. The results showed that the ether oxygens in the soft segment chains are strongly coupled to the potassium or sodium, but much less to cesium. The potentiometric properties of these lipophilic additive doped PU membranes were characterized by incorporating valinomycin and 4‐tert‐butylcalix[4]arene‐tetraacetic acid tetraethylester as potassium‐ and sodium‐selective ionophores, respectively. Their response behavior could be explained by the observed physical characteristics. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 618–625, 2001     

Characteristics of Fe powders prepared by spray pyrolysis from a spray solution with ethylene glycol as the source material of heat pellet

Fe powders as the heat pellet material for thermal batteries are prepared from iron oxide powders obtained by spray pyrolysis from a spray solution of iron nitrate with ethylene glycol. The iron oxide powders with hollow and thin wall structure produce Fe powders with elongated structure and fine primary particle size at a low reducing temperature of 615 °C. The mean size of the primary Fe powders with elongated structure decreases with increasing concentration of ethylene glycol dissolved into the spray solution. The heat pellets prepared from the fine-size Fe powders with elongated structure have good ignition sensitivities below 1 watt. The heat pellets formed from the Fe powders obtained from the spray solution with 0.5 M EG have an extremely high burn rate of 26 cms^?1.     

Aerodynamic performance optimization for the rotor design of a hovering agricultural unmanned helicopter

The importance of using Agriculture unmanned helicopters (AUHs), especially for spraying pesticides and fertilizers on any terrain type to ensure crop yields, has been recently acknowledged. Apart from flying these helicopters at a super-low altitude and low speed, using an efficient and optimum rotor blade ensures a uniform and deep penetration of pesticide and fertilizers over a specified area. Accordingly, this work attempts to optimize the rotor blade of an AUH by using coupling statistics and several numerical techniques, including design of experiments, response surface method, and computational fluid dynamics. The experiments are designed using the central composite design method and by selecting the geometric variables that affect the aerodynamic performance of the rotor blade, including the root chord, tip chord, and angle of attack. The angle at the root and tip is optimized in order for the resulting twist to produce a uniform blade loading, achieve maximum lift, and minimize the required hover power. The required aerodynamic forces and limited availability of engine power are identified as constraints. The blade is optimized only when the helicopter is hovering at a persistent rotational speed, and the hover efficiency of the rotor blade with an optimal twist distribution is significantly higher than the baseline.     

Novel Route to Lead-Based Ferroelectric Compounds via Tetragonal Lead(II) Oxide Intermediates

Single-phase perovskite lead-based ferroelectric powders—Pb(Mg_1/3Nb_2/3)O₃(PMN) or 0.9Pb(Mg_1/3Nb_2/3)O₃–0.1PbTiO₃(0.9PMN–0.1PT)—were prepared using Mg(NO₃)₂, instead of MgO or MgCO₃, via a mixed-oxide method and one-step calcination. The reaction proceeded via the formation of 3Pb(NO₃)₂·7PbO, Pb(OH)₂, tetragonal PbO, and then 2PbO–Nb₂O₅(P₂N) for PMN or 3PbO–Nb₂O₅(P₃N) for PMN–PT; a mixture of PMN and Pb₂(Mg _x Nb_1.33)O_{5.33+ x} then formed, followed finally by the formation of single-phase PMN or 0.9PMN–0.1PT. Such prepared powder showed excellent room-temperature dielectric constants—13800 for PMN or 22600 for 0.9PMN–0.1PT—by sintering at a temperature of 900°C for 2 h.     

A study of the corrosion properties of plasma nitrocarburized and oxidized AISI 1020 steels

Plasma nitrocarburized AISI 1020 steels were oxidized for 15, 30 and 60 min to evaluate their corrosion and microstructural properties. After plasma nitrocarburizing for 3 h at 570°C in a gas mixture comprising 85 vol.% N₂, 12vol.% H₂ and 3 vol.% CH₄, the compound layer composed of ɛ-Fe_2–3(N,C) and γ’-Fe₄(N,C) phases and the diffusion layer above the matrix were observed. The top oxide layer, consisting mainly of magnetite (Fe₂O₄) and hematite (Fe₂O₃) phases, forms after post-oxidation treatment at 500°C. However, the oxide layer was severely degraded by spallation as a result of increases in post-oxidizing time. The difference in corrosion resistance should be attributed to the thickness of the top oxide layer, which was governed by post-oxidizing time.     

Enhanced stability of <Emphasis Type="Italic">Candida antarctica</Emphasis> lipase B in ionic liquids

The activity and stability of lipase from Candida antarctica were investigated in the kinetic resolution of (R,S)-1-phenylethanol with vinyl acetate using ionic liquids (ILs) as reaction media. Among ILs tested, the highest activity of lipase was observed in [Edmim][Tf₂N]. In hydrophobic ILs such as [Edmim][Tf₂N], [Emim][Tf₂N] and [Pmim] [PF₆], lipase could retain its activity after 5 times reuse, while the activity of lipase in hydrophilic ILs and organic solvents was drastically decreased. The activities of lipase in [Edmim][Tf₂N], [Emim][Tf₂N] and [Pmim][PF₆] were also well maintained after 1 day incubation at 80 °C. The lipase suspended in [Edmim][Tf₂N] could be successfully reused 6 times without loss of activity.     

Effects of magnetic field on calcium carbonate precipitation: Ionic and particle mechanisms

There are two most widely reported mechanisms to study the effect of magnetic fields on calcium carbonate (CaCO₃) precipitate, namely ionic and particle mechanisms. The effects are most debatable because they are contrary to each other. This study explored the effects of both mechanisms in CaCO₃ deposit and total CaCO₃ precipitation using ionic and particle methods. The ionic method showed reductions in CaCO₃ deposit and total precipitation rate of CaCO₃, whereas the particle method showed the opposite results. The particle number decreased and the average particle diameter of CaCO₃ deposit increased in the ionic method. Meanwhile in the particle method, the particle number increased, average particle diameter decreased and particle aggregation of CaCO₃ was observed. XRD measurement on all deposits showed that the crystal deposit was mostly of calcite and the traces of vaterite. However, the amount of the crystal in the particle method was observed to be less than that in the ionic method, indicating that CaCO₃ deposit was more amorphous. Particle mechanism decreased the Ca²⁺ ion concentration in solution during magnetization, and ionic mechanism reduced scale (CaCO₃) formation after magnetization and separation processes. This method could be applied for decreasing water hardness and prevent the formation of scaling.     

Autothermal reforming of methane to syngas with palladium catalysts and an electric metal monolith heater

The autothermal reforming of methane to syngas for use in the Fischer-Tropsch synthesis was studied in this work over PdO containing various combinations of CeO₂, BaO or SrO in a washcoated form on a metallic monolith at atmospheric pressure. This study focused on the autothermal operation of the system, in which an electric heater inside the reactor was used only to reach the ignition temperature, and thereafter the autothermal reaction successfully sustained itself without any external heat source. It was concluded from the experiments that the PdO/Al₂O₃ catalyst was better than the others, except for PdO-CeO₂-BaO-SrO/Al₂O₃, which showed similar performance in terms of the CH₄ conversion and H₂+CO selectivity, while affording a higher H₂/CO ratio (close to ca. 3) than the PdO/Al₂O₃ catalyst did (close to ca. 2). The gas hourly space velocity and O₂/CH₄ ratio governed the methane conversion, while the H₂O/CH₄ ratio controlled the H₂/CO ratio. A methane conversion of ∼87%, H₂+CO selectivity of ∼94%, H₂/CO ratio of ∼2.9, and M factor ∼2.15 were obtained under the conditions of a gas hourly space velocity (GHSV) of 120,000 h⁻¹, O₂/CH₄=0.6 and H₂O/CH₄=0.5.