Effect of heat treatment on phase transition of nanotubular titanium oxide arrays

The purpose of this study was to investigate the effects of heat treatment on the cystallinity of titanium nanotubes. The titanium nanotubes had diameters ranging from 90-95 nm, lengths between 400-500 nm, and thicknesses of 11 nm. After heat treatment at high temperatures, the diameter and length of the nanotubes decreased, whereas the thickness increased. The titanium nanotubes exhibited amorphous + anatase phases at 300 degrees C, anatase + rutile phases at 500 degrees C and a rutile phase at 800 degrees C.     

Physical properties and characterization of biodegradable films using nano-sized TiO2/poly(acrylamide-co-methyl methacrylate) composite

In this study, biodegradable films were prepared by using corn starch, PVA, nano-sized poly(acrylamide-co-methyl methacrylate) (PAAm-co-MMA), nano-sized TiO2(P-25)/PAAm-co-MMA composite, and additives which are harmless to the human body, that is, glycerol (GL) and citric acid (CA). Nano-sized PAAm-co-MMA was synthesized by the method of emulsion polymerization. Also, nano-sized TiO2/PAAm-co-MMA composites were synthesized by wet milling for 48 h. The morphology and crystallinty of nano-sized PAAm-co-MMA and TiO2/PAAm-co-MMA composite was observed by the SEM and XRD. The physical properties such as tensile strength (TS), elongation at break (%E), degree of swelling (DS), and solubility (S) of biodegradable films were investigated. The photocatalytic degradability of starch/PVA/nano-sized TiO2/PAAm-co-MMA composite blended films was evaluated using methylene blue as photodegradation target.     

Superconducting toroidal combined-function magnet for a compact ion beam cancer therapy gantry

A superconducting, combined-function, 5 T, 90°, toroidal magnet with a large bore is described in this paper. This magnet is designed to be the last and most difficult part of a compact superconducting magnet-based carbon gantry optics for ion beam cancer therapy. The relatively small size of this toroidal magnet allows for a gantry the size of which is smaller or at least comparable to that of a proton gantry. The gantry design places the toroidal magnet between the scanning magnets and the patient, that is the scanning magnets are placed midway through the gantry. By optimizing the coil winding configuration of this magnet, near point-to-parallel optics is achieved between the scanning magnets and the patient; while at the same time there is only a small distortion of the beam-shape when scanning. We show that the origin of the beam-shape distortion is the strong sextupole components, whose effects are greatly pronounced when the beam is widely steered in the magnet. A method to correct such an undesirable effect is suggested and demonstrated by a numerical particle tracking through the calculated three-dimensional magnetic field.     

Interface effect of magnetic properties in Ni nanoparticles with a hcp core and fcc shell structure

We have fabricated hexagonal close-packed (hcp) Ni nanoparticles covered by a face-centered cubic (fcc) Ni surface layer by polyol method. The magnetic properties have been investigated as a function of temperature and applied magnetic field. The magnetic behavior reveals that the system should be divided magnetically into three distinct phases with different origins. The fcc Ni phase on the shell contributes to the superparamagnetism through a wide temperature range up to 360 K. The hcp Ni phase at the core is associated with antiferromagnetic nature below 12 K. These observations are in good agreement with the X-ray absorption spectroscopy and magnetic circular dichroism measurements. In our particular case, the unique hcp core and fcc shell structure gives rise to an additional anomaly at 20 K in the zero-field-cooled magnetization curve. Its position is barely affected by the magnetic field but its structure disappears above 30 kOe, showing a metamagnetic transition in the magnetization versus magnetic field curve. This new phase originates from the magnetic exchange at the interface between the hcp and fcc Ni sublattices.     

Effect of support size on the catalytic activity of metal-oxide-doped silica particles in the glycolysis of polyethylene terephthalate

Zinc oxide (ZnO) and cerium oxide (CeO2) nanoparticles were deposited on the surface of preformed silica spheres with diameters ranging from 60 to 750 nm. Ultrasonic irradiation was employed to promote the deposition of the metal oxide nanoparticles on the surface of silica. Silica-supported zinc oxide or cerium oxide was used as a catalyst in the glycolysis of polyethylene terephthalate, one of the key processes in the depolymerization of polyethylene terephthalate. The effect of the support size on the catalytic activity was studied in terms of monomer yield, and the monomer concentration was analyzed via high-performance liquid chromatography (HPLC). The morphologies and surface properties of the catalysts were characterized using a scanning electron microscope, a transmission electron microscope, and a BET surface area analyzer, while the monomer was characterized via HPLC and nuclear-magnetic-resonance spectroscopy. Both the zinc oxide and cerium oxide deposited on a smaller support showed better distribution and less aggregation. The high specific surface area of the smaller support catalysts provided a large number of active sites. The highest monomer yield was obtained with a catalyst of 60-nm silica support.     

Lead-free electrostrictive bismuth perovskite ceramics with thermally stable field-induced strains

Electric field-induced strain (EFIS) properties of Bi_1/2(Na_0.82K_0.18)_1/2TiO₃ (BNKT) ceramics modified with Sr(K_1/4Nb_3/4)O₃ (SKN) have been investigated as functions of composition and temperature. BNKT ceramics near a phase boundary revealed the coexistence of ferroelectric rhombohedral and tetragonal phases, resulting in a typical ferroelectric butterfly-shaped bipolar S–E loop at room temperature, whose normalized strain (S_max/E_max) showed a significant temperature coefficient of 0.38 pm/V/K. However, 5 mol% SKN-modified BNKT ceramics revealed a typical electrostrictive behaviour with a thermally stable electrostrictive coefficient, Q₃₃ = 0.021 m⁴/C², which is almost comparable to that of Pb(Mg_1/3Nb_2/3)O₃ (PMN) ceramics that have been dominantly used as Pb-based electrostrictive materials over the last decades.     

Hydrothermal synthesis of PtRu nanoparticles supported on graphene sheets for methanol oxidation in direct methanol fuel cell

Platinum–ruthenium (PtRu) nanoparticles are dispersed on graphene nanosheets and multi-walled carbon nanotubes (MWCNTs) via a hydrothermal method. Transmission electron microsocopy (TEM) observation shows the uniformly dispersed nanoparticles and the average nanoparticle size has been calculated. The electrochemical measurements demonstrate that the Pt–Ru/graphene catalyst exhibits about two times higher mass activity and better tolerance to poisoning species in methanol electro-oxidation than the Pt–Ru/MWCNTs catalyst. This study indicates that the PtRu anodic catalyst synthesized by hydrothermal method can be applied for direct methanol fuel cells (DMFC).     

Kinetics of aluminum dross dissolution in sec-butyl alcohol for aluminum sec-butoxide

Al sec-butoxide (ASB) has been used as a precursor for activated aluminas but its cost is higher than any other type of precursor. This study was carried out on the dissolution kinetics for synthesis of the ASB from Al dross waste. The reaction was performed under the molar ratio of Al dross and sec-butyl alcohol (SBA) of 3 mol SBA/mol Al with a catalyst of 10^?3 mol HgI₂/mol Al and three different dissolution temperatures of 80, 90 and 100 °C. The Al reactant was used with Al dross of 3–5 mm size range. As a result of the experiment, the dissolution reaction gave a 65% yield after 24 h. The dissolution mechanism was determined by the shrinking core model assumed by the shape of spherical particles. Especially, the kinetic data were well fitted by a chemical reaction in the model. By the Arrhenius equation, the apparent activation energy was determined to be 40.9 kJ mol^?1 at the given reaction temperatures.     

Oxidative coupling of methane over Na+-ZrO2-C1-/Al2O3 catalysts

Oxidative coupling of methane (OCM) was carried out over Na⁺-ZrO₂-Cl /A1[₂O₃ catalysts in a temperature range from 1023 to 1123 K. The catalysts were prepared by impregnating the α- or γ-Al₂O₃ supports with sodium carbonate and/or zirconyl chloride. The OCM activity was examined using the catalysts prepared by three different preparation procedures. The best catalyst was the one prepared by subsequent impregnation of sodium carbonate-preimpregnated γ-Al₂O₃ with a mixed solution of sodium carbonate and zirconyl chloride. It was found that preimpregnated sodium played an important role in reducing the combustion activity of the γ-Al₂O₃. The catalyst with an optimal composition showed the highest C₂ selectivity and yield of 40.8% and 15.1%, respectively. From the X-ray diffraction analysis it was found that tetragonal ZrO₂ was formed and that NaCl existed in the catalysts with relatively high sodium contents.     

Effect of Additives on the Electromechanical Properties of Pb(Zr,Ti)O3–Pb(Y2/3W1/3)O3 Ceramics

Dielectric and piezoelectric properties of 0.02Pb(Y_2/3W_1/3)O₃ 0.98Pb(Zr0.52Ti0.48)O3 ceramics doped with additives (Nb₂O₅, La₂O₃, MnO₂, and Fe₂O₃) were investigated. The grain sizes of these ceramics decreased with increasing amounts of additives. For additions of MnO₂ and Fe₂O₃, dielectric losses decreased, while for Nb₂O₅ and La₂O₃, these values increased. The maximum values of the mechanical quality factor Q_m were found to be 956 and 975 for additions of 0.9 wt% Fe₂O₃ and 0.7 wt% MnO₂, respectively, but donor dopants (Nb₂O₅ and La₂O₃) did not change the values of Q_m . On the other hand, the piezoelectric constant d₃₃ and the electromechanical coupling factor k_p decreased with additions of MnO₂ and Fe₂O₃, but improved with additions of Nb₂O₅ and La₂O₃.