Annealing-induced enhancement of ferromagnetism in SnO2-core/Cu-shell coaxial nanowires

In this study, we have coated tin oxide (SnO₂) nanowires with a Cu shell layer via the sputtering method and subsequently investigated the effects of thermal annealing. The annealing-induced changes in morphologies, microstructures, and compositions of the resulting core-shell nanowires were characterized by using scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM), and energydispersive X-ray spectroscopy (EDX). The Cu shell layers were agglomerated to form clusters, which were mainly comprised of the Cu₂O phase. For the first time, a hysteresis loop indicating weak ferromagnetism was observed from the pure SnO₂ nanowires. Both the coercivity and the retentivity in the hysteresis loop were slightly increased by Cu-sputtering, indicating a very slight enhancement of ferromagnetism. Also, the ferromagnetic behavior was significantly enhanced by thermal annealing. We discuss the possible mechanisms of annealing-induced enhancement of ferromagnetism in the SiO₂/Cu core-shell nanowires, which include the generation of Cu₂O phase, Cu-doping into the SnO₂ lattice, and the generation of oxygen vacancies in SnO₂ core nanowires.     

Portable,parallel grid dye-sensitized solar cell module prepared by screen printing

Screen-printing technology is used to fabricate large dye-sensitized solar cells (DSSCs). The high series-resistance associated with transparent conductive oxide glass substrates causes poor performance in large DSSCs especially at an exposure of 1 sun. The DSSC design has an embedded silver grid; a fluorine-doped tin oxide (FTO) glass substrate and stripe type titanium dioxide (TiO₂) active layers introduced by screen-printing. The counter electrode is prepared from a screen printable paste based on hexachloro platinic acid. A DSSC module, which consists of five stripe-type working electrodes on a 5 cm × 5 cm, embedded silver grid FTO glass substrate, shows stable performance with an energy conversion efficiency of 5.45% under standard test conditions.     

Effect of SiO2-ZrO2 supports prepared by a grafting method on hydrogen production by steam reforming of liquefied natural gas over Ni/SiO2-ZrO2 catalysts

SiO₂-ZrO₂ supports with various zirconium contents are prepared by grafting a zirconium precursor onto the surface of commercial Carbosil silica. Ni(20 wt.%)/SiO₂-ZrO₂ catalysts are then prepared by an impregnation method, and are applied to hydrogen production by steam reforming of liquefied natural gas (LNG). The effect of SiO₂-ZrO₂ supports on the performance of the Ni(20 wt.%)/SiO₂-ZrO₂ catalysts is investigated. SiO₂-ZrO₂ prepared by a grafting method serves as an efficient support for the nickel catalyst in the steam reforming of LNG. Zirconia enhances the resistance of silica to steam significantly and increases the interaction between nickel and the support, and furthermore, prevents the growth of nickel oxide species during the calcination process through the formation of a ZrO₂-SiO₂ composite structure. The crystalline structures and catalytic activities of the Ni(20 wt.%)/SiO₂-ZrO₂ catalysts are strongly influenced by the amount of zirconium grafted. The conversion of LNG and the yield of hydrogen show volcano-shaped curves with respect to zirconium content. Among the catalysts tested, the Ni(20 wt.%)/SiO₂-ZrO₂ (Zr/Si = 0.54) sample shows the best catalytic performance in terms of both LNG conversion and hydrogen yield. The well-developed and pure tetragonal phase of ZrO₂-SiO₂ (Zr/Si = 0.54) appears to play an important role in the adsorption of steam and subsequent spillover of steam from the support to the active nickel. The small particle size of the metallic nickel in the Ni(20 wt.%)/SiO₂-ZrO₂ (Zr/Si = 0.54) catalyst is also responsible for its high performance.     

Hydrogen production by steam reforming of liquefied natural gas over a nickel catalyst supported on mesoporous alumina xerogel

Mesoporous alumina xerogel (A-SG) is prepared by a sol–gel method for use as a support for a nickel catalyst. The Ni/A-SG catalyst is then prepared by an impregnation method, and is applied to hydrogen production by steam reforming of liquefied natural gas (LNG). The effect of the mesoporous alumina xerogel support on the catalytic performance of Ni/A-SG catalyst is investigated. For the purpose of comparison, a nickel catalyst supported on commercial alumina (A-C) is also prepared by an impregnation method (Ni/A-C). Both the hydroxyl-rich surface and the electron-deficient sites of the A-SG support enhance the dispersion of the nickel species on the support during the calcination step. The formation of the surface nickel aluminate phase in the Ni/A-SG catalyst remarkably increases the reducibility and stability of the catalyst. Furthermore, the high-surface area and the well-developed mesoporosity of the Ni/A-SG catalyst enhance the gasification of surface hydrocarbons that are adsorbed in the reaction. In the steam reforming of LNG, the Ni/A-SG catalyst exhibits a better catalytic performance than the Ni/A-C catalyst in terms of LNG conversion and hydrogen production. Moreover, the Ni/A-SG catalyst shows strong resistance toward catalyst deactivation.     

CO2 bubble absorption enhancement in methanol-based nanofluids

In this study, the nanoparticles (i.e. SiO₂ and Al₂O₃ nanoparticles) and methanol are combined into SiO₂/methanol and Al₂O₃/methanol nanofluids to enhance the CO₂ absorption rate of the base fluid (methanol). The absorption experiments are performed in the bubble type absorber system equipped with mass flow controller (MFC), mass flow meter (MFM) and silica gel (which can remove the methanol vapor existing in the outlet gases). The parametric analysis on the effects of the particle species and concentrations on CO₂ bubble absorption rate is carried out. The particle concentration ranges from 0.005 to 0.5 vol%. It is found that the CO₂ absorption rate is enhanced up to 4.5% at 0.01 vol% of Al₂O₃/methanol nanofluids at 20 °C, and 5.6% at 0.01 vol% of SiO₂/methanol nanofluids at −20 °C, respectively.     

Synthesis of polyaniline-gold/graphene oxide composite and microwave absorption characteristics of the composite films

This paper describes the synthesis of polyaniline-gold nanocomposite by an in situ polymerization of aniline hydrochloride with graphene oxide using hydrogen tetrachloroaurate as an oxidant. The synthesized nanocomposites were characterized by FT-IR and UV–vis spectroscopy, and their surface morphology was studied by scanning and transmission electron microscopy. Microwave absorption property of the composite films was studied at 2–12 GHz, and the effects of sample thickness on the microwave absorption were investigated. The electromagnetic interference shielding effectiveness of PANI-GNP has been enhanced due to the inclusion of GO.     

Preparation of hydroxyapatite-carbon nanotube composite nanopowders

Here we report a simple preparation of composite nanopowders made of hydroxyapatite (HA) and carbon nanotube (CNT). In particular, CNTs were ionically modified to dissolve homogeneously in a series of organic solvents, including tetrahydrofuran and ethanol. The addition of HA nanopowders within the CNTs solution resulted in rapid precipitation of the composite HA-CNTs nanopowders. High resolution electron image revealed individual CNTs were evenly distributed within the cluster of HA nanoparticulates. A maximal concentration of CNTs to be organized within the HA nanopowder was highly dependent on the physicochemical characteristics of HA powders. A pilot biological assessment of the composite powders demonstrated favorable adhesion and growth of tissue cells. The developed HA-CNTs composite nanopowders may be potentially useful as an initial powder source for HA-CNT nanocomposites or coatings in biomedical applications.     

Synthesis and characterization of soluble polypyrrole–poly(ɛ-caprolactone) polymer blends with improved electrical conductivities

Polypyrrole–poly(?-caprolactone) (PPy–PCL) blends were prepared through an in situ deposition technique wherein different amounts of poly(?-caprolactone) were added during the polymerization of pyrrole. Ammonium persulfate was used as an oxidant in the polymerization of polypyrrole (PPy). Compared with pure PPy, the blends showed higher solubility in many organic solvents. The composition and structural characteristics of PPy–PCL were determined by Fourier transform infrared, ultraviolet–visible, and X-ray photoelectron spectroscopic methods. Scanning electron and transmission electron microscopic methods were performed to observe the morphology of the PPy–PCL blends. The temperature-dependent conductivity of the PPy–PCL blends was measured at 300–500 K. The conductivity increased with increasing PCL concentration in the blends, which can be explained by the increased mobility of charge carriers at high PCL concentrations. Based on the temperature dependence of the electrical conductivity, hopping may be the conduction mechanism involved in the PPy–PCL blending process.     

Hazardous phytotoxic nature of cobalt and zinc oxide nanoparticles assessed using Allium cepa

The increasing use of nanotechnology requires the clarification of the behavior and the effects of nanoparticles (NPs) as they are released into the environment. This study was to investigate the phytotoxicity of cobalt and zinc oxide NPs using the roots of Allium cepa (onion bulbs) as an indicator organism. The effects of cobalt and zinc oxide NPs on the root elongation, root morphology, and cell morphology of a plant, as well as their adsorption potential, were determined through the hydroponic culturing of A. cepa. A. cepa roots were treated with dispersions of the cobalt and zinc oxide NPs having three different concentrations (5, 10, and 20 μg ml(-1)). With increasing concentrations of the NPs, the elongation of the roots was severely inhibited by both the cobalt and the zinc oxide NPs as compared to that in the control plant (untreated A. cepa roots). Massive adsorption of cobalt oxide NPs into the root system was responsible for the phytotoxicity. Zinc oxide NPs caused damage because of their severe accumulation in both the cellular and the chromosomal modules, thus signifying their highly hazardous phytotoxic nature.