Reinforcement of rigid PVC/wood‐flour composites with multi‐walled carbon nanotubes

Multi‐walled carbon nanotubes (CNT) were compounded with PVC by a melt blending process based on fusion behaviors of PVC. The effects of CNT content on the flexural and tensile properies of the PVC/CNT composites were evaluated in order to optimize the CNT content. The optimized CNT‐reinforced PVC was used as a matrix in the manufacture of wood‐plastic composites. Flexural, electrical, and thermal properties of the PVC/wood‐flour composites were evaluated as a function of matrix type (nonreinforced vs. CNT‐reinforced). The experimental results indicated that rigid PVC/wood‐flour composites with properties similar to those of solid wood can be made by using CNT‐reinforced PVC as a matrix. The CNT‐reinforced PVC did not influence the electrical and thermal conductivity of the PVC/wood‐flour composites. J. VINYL ADDIT. TECHNOL., 2008. © 2008 Society of Plastics Engineers.     

Heterogeneous catalytic degradation of cyanide using copper-impregnated pumice and hydrogen peroxide

The main objective of this research was to investigate the oxidative destruction of free cyanide with hydrogen peroxide and copper-impregnated pumice as a heterogeneous catalyst. Original or copper-impregnated pumices added alone were not effective adsorbents of negatively charged cyanide ions due to incompatible surface interactions. Peroxide and original pumices added together were also ineffective in removing cyanide. However, for all of the three natural pumices tested with various particle size fractions, the use of copper-impregnated pumices and peroxide together significantly enhanced both the initial rate and extent of cyanide removal. Although copper-impregnated specific surface area was the major factor affecting the rate and extent of cyanide destruction for a particular pumice source with similar surface chemistries, the type of surface chemistry (i.e., specific functional groups) within different pumice sources also appears to be a very important factor. Lower rates and extents of cyanide removals were observed at pH 11 compared to pH 8 probably because of the negative impacts of alkaline conditions in terms of scavenging peroxide and forming more negatively charged pumice surfaces. Both the initial rate and ultimate extent of cyanide removals were generally higher at a temperature of 20 degrees C compared with those found at 10 degrees C. The use of copper-impregnated pumice as a light, cheap, readily available, natural, and porous heterogeneous catalyst either in completely mixed/suspended or fixed-bed reactor configurations may be an effective treatment technology for cyanide removal from solution. This new approach may minimize downstream metal removal problems experienced in conventional cyanide oxidation technologies.     

添加铈对高压压铸AM50镁合金显微组织和力学性能的影响

研究添加铈对高压压铸AM50镁合金显微组织和力学性能的影响.结果表明:添加铈能使AM50镁合金晶粒细化,并使其室温和高温力学性能得到显著改善.相对于未添加Ce和添加0.5％Ce(质量分数)的AM50镁合金,添加1％Ce(质量分数)的镁合金的晶粒更细,力学性能更优.     

α‐Thiophene end‐capped styrene copolymer containing fullerene pendant moieties: Synthesis,characterization, and gas sensing properties

We report the synthesis, characterization, and gas sensing properties of a styrene copolymer bearing α‐thiophene end group and fullerene (C₆₀) pendant moieties P(S‐co‐CMS‐C₆₀). First, the copolymer of styrene (S) and chloromethylstyrene (CMS) monomers was prepared in bulk via a bimolecular nitroxide‐mediated radical polymerization (NMP) technique using benzoyl peroxide (BPO) as the radical initiator and nitroxy‐functional thiophene compound (Thi‐TEMPO) as the co‐radical and this gave α‐thiophene end‐capped copolymer P(S‐co‐CMS). The chloromethylstyrene units of P(S‐co‐CMS) allowed further side‐chain functionalization onto P(S‐co‐CMS). The obtained P(S‐co‐CMS) was then reacted with sodium azide (NaN₃) and this led to the copolymer with pendant azide groups, P(S‐co‐CMS‐N₃), and then grafted with electron‐acceptor C₆₀ via the reaction between N₃ and C₆₀. The final product was characterized by using NMR, FTIR, and UV–vis methods. Electrical characterization of P(S‐co‐CMS‐C₆₀) thin film was also investigated at between 30 and 100 °C as the ramps of 10 °C. Temperature dependent electrical characterization results showed that P(S‐co‐CMS‐C₆₀) thin film behaves like a semiconductor. Furthermore, P(S‐co‐CMS‐C₆₀) was employed as the sensing layer to investigate triethylamine (TEA), hydrogen (H₂), acetone, and ethanol sensing properties at 100 °C. The results revealed that P(S‐co‐CMS‐C₆₀) thin film has a sensing ability to H₂. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43641.     

Effects of sheet thickness and anisotropy on forming limit curves of AA2024-T4

In this study, the effects of sheet thickness and anisotropy of AA2024-T4 on forming limit curve (FLC) are experimentally investigated according to ISO 12004-2 standard. A new limit strain measurement method is proposed by using the grid analysis method so as to determine limit strains conveniently and reliably. In addition to the regular test specimens, various widths are added to enhance the FLC’s accuracy at the plane strain condition (PSC). The accuracy and reliability of the proposed method are verified for different materials. Results illustrate that an increase in the sheet thickness increases the FLC level. The additional experiments for additional widths improve the accuracy of the FLC at the PSC, and the position of the lowest major strain value differs from the literature. However, the effect of anisotropy on the FLC is found to be insignificant. Finally, experimental and numerical case studies are carried out for conventional deep drawing, stretch drawing, and hydraulic bulge processes. Results reveal that different FLCs are necessary for different thicknesses for accurate predictions.     

Electrochemical synthesis and characterization of poly(9-benzylfluorene)

In this study, we report the electrochemical polymerization of 9-benzylfluorene (9-BF) in acetonitrile solution. The characterization of the resulting poly(9-BF) film obtained on the working electrode has been performed by using attenuated total reflectance infrared spectroscopy. Besides electrochemical properties, the optical and photoluminescent properties of film were also investigated in detail by means of UV–Vis spectroscopy and fluorescence spectroscopy. Fluorescent spectral studies indicate that polymer film in solid state emits blue-green light at around 470/520 nm under irradiation of UV light. In addition, scanning tunneling microscopy was used to investigate the morphology of poly(9-BF) film. The morphological results also reveal that the surface of single crystalline gold electrode is completely covered with the polymer film.     

Waste Mg-Al based alloys for hydrogen storage

Magnesium has been studied as a potential hydrogen storage material for several decades because of its relatively high hydrogen storage capacity, fast sorption kinetics (when doped with transition metal based additives), and abundance. This research aims to study the possibility to use waste magnesium alloys to produce good quality MgH₂. The production costs of hydrogen storage materials is still one of the major barriers disabling scale up for mobile or stationary application. The recycling of magnesium-based waste to produce magnesium hydride will significantly contribute to the cost reduction of this material. This study focuses on the effect of different parameters such as the addition of graphite and/or Nb₂O₅ as well as the effect of milling time on the material hydrogenation/de-hydrogenation performances. In addition, morphology and microstructural features are also evaluated for all the investigated materials.     

Influences of Boundary Condition on Laminar Natural Convection of Bingham Fluids in Square Cross-Sectioned Cylindrical Annular Enclosures with Differentially Heated Vertical Walls

Numerical simulations have been carried out to analyze steady-state laminar natural convection of yield stress fluids obeying Bingham model in square cross-sectioned cylindrical annular enclosures with differentially heated vertical walls for both constant wall temperature and constant wall heat flux boundary conditions for active walls. The simulations have been performed under the assumption of axisymmetry for a nominal Rayleigh number range of 10³ to 10⁶ and nominal Prandtl number range of 10 to 10³ for different ratio of internal cylinder radius to cylinder height range of 0.125 to 16. The mean Nusselt number on the inner periphery for the constant wall heat flux configuration has been found to be smaller than that in the case of constant wall temperature configuration for a given set of values of nominal Rayleigh and Prandtl numbers for both Newtonian and Bingham fluid cases. The mean Nusselt number normalized by the corresponding value obtained for pure conductive transport increases with increasing internal radius before approaching the corresponding mean Nusselt number for square enclosures regardless of the boundary conditions. Detailed physical explanations have been provided for the effects of the aforementioned parameters on the mean Nusselt number on the inner periphery. Finally, the new Nusselt number correlations have been proposed for laminar natural convection of both Newtonian and Bingham fluids in square cross-sectioned cylindrical annular enclosures for both constant wall temperature and constant wall heat flux boundary conditions.     

Preparation and characterization of Ni based catalysts for the catalytic partial oxidation of methane: Effect of support basicity on H2/CO ratio and carbon deposition

The catalytic partial oxidation of methane (CPOM) was studied on Ni based catalysts. Catalysts were prepared by wet impregnation method and characterized by using AAS, BET, XRD, HRTEM, TPR, TPO, Raman Spectroscopy and TPSR techniques. The prepared catalysts showed nearly 95% CH₄ conversion and nearly 96% H₂ selectivity under the flow of 157,500 (L kg⁻¹ h⁻¹) with the ratio of CH₄/O₂ = 2 by using air as an oxidant at 1 atm and 800 °C. Support basicity greatly influenced the H₂/CO ratio and carbon deposition. It was found that the lowest carbon deposition occurred on Ni impregnated MgO catalyst. Considering the results, it was found that Ni/MgO catalyst with 10% Ni content would be the best catalyst amongst Ni/Al₂O₃, Ni/MgO/Al₂O₃, Ni/MgAl₂O₄ and Ni/Sorbacid for the CPOM only under more reductive conditions. Under optimum conditions, Ni/MgO showed poor performance and therefore Ni/Sorbacid would be the ideal catalyst because of its greater carbon resistance than the other catalysts.     

Self-assembly of highly charged polyelectrolyte complexes with superior proton conductivity and methanol barrier properties for fuel cells

The paper is concerned with the formation of Layer-by-Layer (LbL) self-assembly of highly charged polyvinyl sulfate potassium salt (PVS) and polyallylamine hydrochloride (PAH) on Nafion membrane to obtain the multilayered composite membranes with both high proton conductivity and methanol blocking properties. Also, the influences of the salt addition to the polyelectrolyte solutions on membrane selectivity (proton conductivity/methanol permeability) are discussed in terms of controlled layer thickness and charge density.The deposition of the self-assembly of PAH/PVS is confirmed by SEM analysis and it is observed that the polyelectrolyte layers growth on each side of Nafion membrane regularly. (PAH/PVS)₁₀-Na⁺ and (PAH/PVS)₁₀-H⁺ with 1.0 M NaCl provide 55.1 and 43.0% reduction in lower methanol permittivity in comparison to pristine Nafion, respectively, while the proton conductivities are 12.4 and 78.3 mS cm⁻¹. Promisingly, it is found that the membrane selectivity values (Φ) of all multilayered composite membranes in H⁺ form are much higher than those of Na⁺ form and perfluorosulfonated ionomers reported in the literature. These encouraging results indicate that composite membranes having both superior proton conductivity and improved methanol barrier properties can be prepared from highly charged polyelectrolytes including salt for fuel cell applications.