Assessment of CpTi Surface Properties after Nitrogen Ion Implantation with Various Doses and Energies

Nitrogen ion implantation is one of the surface modification techniques used for increasing corrosion resistance of commercially pure titanium (CpTi). The nitrogen ion implanted CpTi in various doses markedly changes the corrosion resistance. Still the effect of nitrogen ion implantation on the CpTi at different energies needs to be verified. This study uses different methods to assess the CpTi surface properties after nitrogen ion implantation in various doses and energy. Surface hardness of the CpTi increases with an increase of the dose and decreases with an increase of the energy. The precipitation of the TiN increases with an increase of the nitrogen dose, and no formation of the Ti₂N phase clearly appears. Corrosion resistance of the CpTi specimens can be upgraded to some extent after their surfaces are modified, implanting nitrogen ions at 100?keV by increasing dose. The optimum surface properties of the implanted CpTi are analyzed to contribute to materials science technology.     

Effects of powder size and metallic bonding layer on corrosion behaviour of plasma-sprayed Al2O3-13% TiO2 coated mild steel in fresh tropical seawater

This study focuses on the effects of powder size and Ni–Al bonding layer on the electrochemical behaviour of plasma-sprayed Al₂O₃-13% TiO₂ coating in fresh tropical seawater. The presence of the metallic bonding layer reduces the coating porosity and increases the surface roughness for both microparticle and nanoparticle coatings. The nanoparticle exhibits better corrosion rate of 1.9×10⁻⁶ mmpy compared to the microparticle coating, with a corrosion rate of 3.05×10⁻⁶ mmpy. However, the presence of the metallic bonding layer increases the corrosion rate for both micro and nanoparticle coatings. The corrosion mechanism for the coating with and without the metallic bonding layer is discussed in detail.     

Synthesis of gallium nitride nanostructures by nitridation of electrochemically deposited gallium oxide on silicon substrate

Gallium nitride (GaN) nanostructures were successfully synthesized by the nitridation of the electrochemically deposited gallium oxide (Ga₂O₃) through the utilization of a so-called ammoniating process. Ga₂O₃ nanostructures were firstly deposited on Si substrate by a simple two-terminal electrochemical technique at a constant current density of 0.15 A/cm² using a mixture of Ga₂O₃, HCl, NH₄OH and H₂O for 2 h. Then, the deposited Ga₂O₃ sample was ammoniated in a horizontal quartz tube single zone furnace at various ammoniating times and temperatures. The complete nitridation of Ga₂O₃ nanostructures at temperatures of 850°C and below was not observed even the ammoniating time was kept up to 45 min. After the ammoniating process at temperature of 900°C for 15 min, several prominent diffraction peaks correspond to hexagonal GaN (h-GaN) planes were detected, while no diffraction peak of Ga₂O₃ structure was detected, suggesting a complete transformation of Ga₂O₃ to GaN. Thus, temperature seems to be a key parameter in a nitridation process where the deoxidization rate of Ga₂O₃ to generate gaseous Ga₂O increase with temperature. The growth mechanism for the transformation of Ga₂O₃ to GaN was proposed and discussed. It was found that a complete transformation can not be realized without a complete deoxidization of Ga₂O₃. A significant change of morphological structures takes place after a complete transformation of Ga₂O₃ to GaN where the original nanorod structures of Ga₂O₃ diminish, and a new nanowire-like GaN structures appear. These results show that the presented method seems to be promising in producing high-quality h-GaN nanostructures on Si.     

Molecular Weight Determination of Palm Olein Polyols by Gel Permeation Chromatography Using Polyether Polyols Calibration

Natural oil polyols have been intensively developed and successfully used for the production of various polymers, notably polyurethanes. The need to access the average molecular weight (MW) and the MW distribution (MWD) has led to the efforts to have a precise and reliable determination method. A series of commercial polyether polyols, with well‐defined MW, was used as a gel permeation chromatography (GPC) calibration standard to determine the MW of palm olein polyols. This GPC analysis was compared to the one calibrated against the commercially available polystyrene (PS) standards and to the number‐average molecular weight (M_n) obtained via vapor pressure osmometry (VPO) technique. For example, the M_n obtained for palm olein polyol E‐135 calibrated against polyether polyols was 2,537 Da, which was closer to the M_n via VPO (1,618 Da), than the M_n obtained using PS as calibration standards (3,836 Da). Hence, this GPC analysis using polyether polyols as calibration standards can offer reassured determination of MWD of palm olein polyols.     

Determination of iodine value of palm oil based on triglyceride composition

The triglyceride (TG) composition of palm oil is normally determined by high-performance liquid chromatography (HPLC). The HPLC chromatograms indicated a good separation of most of the TG components in the oil. The TG can be classified based on either the TG groups, i.e., triunsaturated, monosaturated, disaturated, or trisaturated, or the number of double bonds, i.e., zero, one, two, three, or four double bonds. The more unsaturated the fatty acid, the greater the iodine value (IV). Therefore, it is hypothesized that the IV of an oil can be determined based upon the TG composition of the oil. Based on the TG groups, stepwise regression analysis showed that the areas of the disaturated, trisaturated, and triunsaturated TG peaks could predict the IV with a coefficient of determination (R ²) of 0.990. The regression based on the number of double bonds yielded a good regression equation with R ²=0.992. The important variables were the peak area of the fatty acids that contained zero, one, two, and three double bonds. This study concludes that the TG composition can be used to predict the IV of palm oil. The best prediction model is obtained by using the number of double bonds in the TG as the independent variable.     

Hole Spin Polarization in Metallic Ferromagnetic GaMnAs Multilayers and Superlattices: Lateral and Bloch Miniband Transport

It is shown that spin-polarized currents occur in metallic and ferromagnetic Ga_1–x Mn _x As/GaAs multilayered structures, as a result of the magnetic interaction between holes and the Mn ions. The magnetic layers act as potential barriers for holes with spins aligned parallel to the layer magnetization, and as potential wells for the inverse spin polarization. In the case of currents in-plane, holes with spin parallel and antiparallel to this magnetization move in different regions. By choosing properly the magnetic and the nonmagnetic layers widths, a spin-polarized transport with a difference of an order of magnitude on the mobilities for each spin polarization is predicted to occur. Spin-polarized minibands are also shown to occur in a superlattice based on the same structure. We calculated the dependence of the spin polarization with the superlattice parameters, and we discuss how this polarization affects the Bloch miniband transport in such ferromagnetic superlattice.     

Single-Particle Relaxation Time of the Two-Dimensional Spin-Polarized Electron Gas

We present results for the single-particle relaxation time of the spin-polarized two-dimensional electron gas in Silicon-MOSFET systems at zero temperatures. Spin-polarization is produced by the application of a parallel magnetic field. The single-particle relaxation time was measured with the Shubnikovde–Hass effect and is in good agreement with our theoretical results.     

Studies with microgels as matrices for molecular receptor and catalytic sites: stereoselectivity of copolymers of (−)-menthyl acrylate and N-methacryloyl-hydroxylamineversus chiral esters

The reactivity of 4-nitrophenyl esters has been studied against an optically active microgel copolymer containing hydroxamic acid pendant groups. Saturation phenomena are observed in the kinetics consistent with formation of a complex followed by reaction of the ester in the complexed species. The polymer discriminates between R- and S-forms of a chiral substrate in both complexing and catalytic steps. The data are consistent with the existence of chiral spaces in the microgel bead which accept the chiral substrate. The selectivity of the polymer for the chiral substrate (α ～ 2) compares favourably with that shown by conventional chiral chromatographic supports.