Synthesis and Characterization of Nano-Composite Alumina–Titania Ceramic Membrane for Gas Separation

A ceramic composite membrane was prepared using a commercial titania ceramic membrane coated by alumina oxide via a sol–gel technique where polyvinyl alcohol (PVA) was used as a binder. The characteristic of the membrane was analyzed in terms of the effect of PVA concentration and sintering temperature on viscosity, pore size, density, porosity and surface area of the membrane. Two vol% of PVA solution containing 4 g of PVA in 100 mL of water was adequate to achieve an appropriate porosity level to avoid cracks on the gel layer. Sol viscosity and pore size of the membrane essentially increased when the PVA concentration was increased. The density of the membrane increased as the sintering temperature increased. The porosity level however, decreased when the temperature was increased. The composite membrane was further characterized in terms of permeability of pure gas at low-temperature region (301 K) where an experimental platform has been developed to perform the permeability studies.     

Energy requirement of ultraviolet and AOPs for the post-treatment of treated combined industrial effluent

Post-treatment was carried out to eliminate the colour and COD of treated combined industrial effluent. Ozonation at a dose of 300 mg/h for 10 min resulted in 100% colour and 96% COD removal at pH 8 and temperature 25 °C. The application of UV/H₂O₂ resulted in 91% colour and 82% COD removal. 79% colour and 60% COD removal was obtained with the Fenton process after 60-min treatment in the presence of 170 mg/l H₂O₂, while the photo-Fenton process showed an almost complete elimination of both parameters. Electrical energy consumption showed that the photo-Fenton resulted in the highest removal efficiency with 95% removal in terms of colour and COD abatement rates. The electrical energy requirements of the tested processes followed the increasing order UV/Fe/H₂O₂ < O₃ < UV/H₂O₂ < UV.     

(2S,12Z)-2-Acetoxy-12-heptadecene: Major Sex Pheromone Component of Pistachio Twig Borer, Kermania pistaciella

The sex pheromone of the pistachio twig borer, Kermania pistaciella (Lepidoptera: Oinophilidae), one of the most important insect pests of pistachio, Pistacia vera, in Turkey and Iran, was identified. In gas chromatographic-electroantennographic detection (GC-EAD) and GC-mass spectrometric analyses of pheromone gland extracts of female K. pistaciella from Turkey, (2S,12Z)-2-acetoxy-12-heptadecene was identified as the major candidate pheromone component. In field experiments in Turkey, lures containing synthetic (2S,12Z)-2-acetoxy-12-heptadecene attracted large numbers of male moths. Its attractiveness was significantly reduced by the presence of the R-enantiomer or of either enantiomer of the corresponding alcohol. (2S,12Z)-2-Acetoxy-12-heptadecene is the first pheromone component identified in the Oinophilidae and the first secondary acetate pheromone component identified in the Lepidoptera. An erratum to this article can be found at     

Energy storage capacity investigation of pulsed current formed nano-structured lead dioxide

An electro-deposition method was used for the preparation of nano-structured lead dioxide. The lead dioxide films prepared were used as positive electrodes of lead acid batteries. Different parameters such as pulse time (t_on), pulse height, and relaxation time (t_off) were optimized to obtain higher capacity. Depend on the pulse conditions, a range of different morphologies of various porosities and connectivity was obtained. The resulting batteries were discharged to a cut off voltage of 1.75 V by a pulsed current method. The energy storage ability of the prepared lead acid batteries shows a close relation with the morphology of cathode materials. Maximum capacity was observed when pulse and relaxation time was equal to 0.1 and 5 s, respectively, at a current density of 25 mA cm⁻². A change in morphology of lead dioxide from aggregated globular structure to nanofiber was occurred. It was found that the high surface area as well as high connectivity between particles resulted in increased discharge capacity. Analysis of electrochemical impedance spectroscopy (EIS) data revealed that the charge transfer resistance is decreased by a change in morphology from bulk globular to nanofiber as the energy storage test showed. The time dependence of impedance behavior of a sample prepared at t_on = 0.1 s and t_off = 5 s at 25 mA cm⁻² was investigated and the results are discussed.     

Effect of Addition of Ni metal catalyst onto the Co and Fe supported catalysts for the formation of carbon nanotubes

Production of novel porous material is a major target in current material science research due to its wide applications. As carbon nanotube (CNTs) is a one dimensional hollow structure it is also one of the promising materials in applications ranging from electronics to hydrogen storage medium. Catalytic chemical vapor deposition (CCVD) is a method whereby CNTs can be produced in large amount. Thus, in this work, we have synthesized CNTs via pyrolysis of acetylene using various supported transition-metal catalysts in a fixed-bed reactor. Scanning electron microscope (SEM) and transmission electron microscope (TEM) were used to investigate the CNTs structure. The structures of nanotubes formed by acetylene pyrolysis were dependent on the catalysts used. It was found that alumina supported Ni/Fe catalyst inhibited the formation of CNTs growth while alumina supported Ni/Co catalyst gave high density of CNTs. However, nanotubes grown over alumina supported Ni/Fe catalyst were less dense due to the deactivation of the catalyst at the early stage of the pyrolysis process.     

Rubber‐toughened polypropylene nanocomposite: Effect of polyethylene octene copolymer on mechanical properties and phase morphology

Rubber‐toughened polypropylene (PP)/org‐Montmorillonite (org‐MMT) nanocomposite with polyethylene octene (POE) copolymer were compounded in a twin‐screw extruder at 230°C and injection‐molded. The POE used had 25 wt % 1‐octene content and the weight fraction of POE in the blend was varied in the range of 0–20 wt %. X‐ray diffraction analysis (XRD) revealed that an intercalation org‐MMT silicate layer structure was formed in rubber‐toughened polypropylene nanocomposites (RTPPNC). Izod impact measurements indicated that the addition of POE led to a significant improvement in the impact strength of the RTPPNC, from 6.2 kJ/m² in untoughened PP nanocomposites to 17.8 kJ/m² in RTPPNC containing 20 wt % POE. This shows that the POE elastomer was very effective in converting brittle PP nanocomposites into tough nanocomposites. However, the Young's modulus, tensile strength, flexural modulus, and flexural strength of the blends decreased with respect to the PP nanocomposites, as the weight fraction of POE was increased to 20 wt %. Scanning electron microscopy (SEM) was used for the investigation of the phase morphology and rubber particles size. SEM study revealed a two‐phase morphology where POE, as droplets was dispersed finely and uniformly in the PP matrix. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3441–3450, 2006     

Measurements of Stress Intensity Factors of an Interface Crack Under Mixed Mode Loading

The optical method of caustics has been utilised to measure both the stress intensity factor for a crack lying along the interface of an aluminium/epoxy bimaterial specimen, and the mode mixity arising from the difference in the elastic properties across the interface. Measurements were carried out by using a novel modification to the method whereby caustics are produced and measured from both sides of the specimen, so compensating automatically for the distortion induced in the specimen due to misaligned loading fixtures. A flat reflective surface across the interface was obtained by adhering a reflective coating to the specimen. Verification that this coating does not affect measurement accuracy was obtained by comparing stress intensity factors measured from coated and uncoated monolithic aluminium specimens where good agreement was found to exist between both measurements.     

Modification of glass ionomer cement by incorporating hydroxyapatite-silica nano-powder composite: Sol–gel synthesis and characterization

A nanohydroxyapatite–silica powder was synthesized using an ethanol based sol–gel technique. The synthesized powder was incorporated into commercial glass ionomer powder (Fuji II GC) and characterized using FTIR, ²⁹Si CP/MAS NMR, EDX and XRD spectroscopy. ²⁹Si CP/MAS NMR results showed the presence of higher degree of cross-linking of silyl species between silica and GIC, which makes the Nano-HA–Silica–GIC composite much stronger. High-resolution transmission electron microscopy (TEM) and scanning electron microscopy (TEM) was employed to investigate the morphology of the synthesized powder. Results revealed that higher content of nanosilica produced a denser and stronger GIC. Thus, the application of nanohydroxyapatite–silica–GIC with improved properties are envisioned to be of great clinical importance, especially in stress bearing areas.     

Microwave irradiated and thermally heated olive stone activated carbon for nickel adsorption from synthetic wastewater: A comparative study

In attempt to compare the removal efficiency and yield of the activated carbon prepared using the conventional and microwave‐assisted heating is the focus of this work. Toward this olive stone (a biomass precursor) is activated using the popular activating agent potassium hydroxide. The process optimization exercise is carried out by using the standard full factorial statistical design of experiments (response surface methodology). The activated carbons prepared under the optimized conditions are compared based on the adsorption capacity and yield. The adsorption capacity was found higher using microwave heating as compared with conventional heating. The microwave heating requires significantly lesser holding time as compared to conventional heating method to produce activated carbon of comparable quality, with higher yield. The BET surface area of carbon using microwave heating is significantly higher than the conventional heating. Although the mesopore surface area of carbon is not vary significantly, the activation time, power, and nitrogen gas consumption are significantly lower than the conventional heating rendering that the activation process via microwave is more economical than that via conventional heating. The adsorption isotherm data fitted the Langmuir isotherm well and the monolayer adsorption capacity was found to be 12.0 and 8.42 mg/g for microwave and thermally heated activated carbon, respectively. Regeneration studies showed that microwave‐irradiated and thermally heated olive stone could be used several times by desorption with an HCl reagent. Both carbons can be used for the efficient removal of Ni²⁺ (>99%) from contaminated wastewater. © 2013 American Institute of Chemical Engineers AIChE J, 60: 237–250, 2014     

Characterization and mechanical properties of exfoliated graphite nanoplatelets reinforced polyethylene terephthalate/polypropylene composites

Recently, graphene and its derivatives have been used to develop polymer composites with improved or multifunctional properties. Exfoliated graphite nanoplatelets (GNP) reinforced composite materials based on blend of polyethylene terephthalate (PET), and polypropylene (PP) compatibilized with styrene–ethylene–butylene–styrene‐g‐maleic anhydride is prepared by melt extrusion followed by injection molding. Characterization of the composites' microstructure and morphology was conducted using field emission scanning electron microscopy, transmission electron microscopy (TEM), X‐ray diffraction analysis (XRD), and Fourier transform infrared spectroscopy (FTIR). Tensile and impact strengths of test specimens were evaluated and the results showed maximum values at 3phr GNP in both the cases. Morphological studies showed that the GNPs were uniformly dispersed within the matrix. Results from XRD analysis showed uniformly dispersed GNPs, which may not have been substantially exfoliated. FTIR spectroscopy did not show any significant change in the peak positions to suggest definitive chemical interaction between GNP and the matrix. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40582.