Surface property change of C doped TiO2 nano-pillars by O2 plasma treatment

TiO2 surface is led to super-hydrophilic surface by modifying to hydroxyl group. The super-hydrophilic surface can be applied to anti-fogging, because of preventing formation of water droplet on the surface. Super-hydrophilic coatings are made of metal oxides, polymers, or their mixtures. In this study, columnar-structured C doped TiO2 nano-pillars were grown on glass substrates by MOCVD method. For change of surface properties, grown columnar-structured C-TiO2 nano-pillars were treated by oxygen plasma. After oxygen plasma treatment, the surface property of grown columnar structured C-TiO2 nano-pillars changed from hydrophobic surface to super hydrophilic surface. For determination of this mechanism, scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), FT-IR spectroscopy, and contact angle analyzer were employed.     

Role of O2/Ar mixing ratio on the performances of IZO thin film transistors fabricated using a two-step deposition process

In this study, a simple method of fabricating a thin-film transistor (TFT) with a double-layered channel using indium–zinc-oxide (IZO) films was proposed. Two IZO films used as channel layers were consecutively deposited via sputtering without stopping the vacuum and only by changing the volumetric fraction of the additive O₂ gas during the deposition. Time-of-flight secondary ion mass spectrometry (ToF-SIMS) analysis showed a large difference in the depth profiles of the InO^? and InO₂^? ions between the two IZO layers. Compared to the conventional single-IZO-channel TFT, the double-IZO-channel TFT that was fabricated using the proposed two-step deposition method showed greatly improved electrical characteristics: the on/off-state current ratio was increased from 1.30 × 10⁵ to 1.03 × 10⁶, and the field effect mobility was enhanced from 1.2 to 9.3 cm²/Vs.     

Enhanced dielectric and piezoelectric properties of low-temperature processed Pb(Zr,Ti)O3 thick films prepared by hybrid deposition technique with chemical solution infiltration process

High quality PZT thick films over 10 μm were successfully prepared using a chemical solution infiltration into the porous screen-printed PZT thick films. The hybrid films prepared with solution infiltration process showed very dense and uniform microstructure with large grain size at a low annealing temperature such as 700 °C. The hybrid films showed markedly enhanced electrical properties. The measured dielectric constant, the remanent polarization and the piezoelectric d₃₃ coefficient of the films were 1900, 27 μC/cm², and 230 pC/N, respectively, which were over two times higher than those of the screen printed films without the solution infiltration process.     

Novel SrCo1 − 2x(Fe,Nb)xO3 − δ (x = 0.05, 0.10) oxides targeting CO2 capture and O2 enrichment: Structural stability and oxygen sorption properties

The novel Fe/Nb co-doped SrCo_1 ? 2x(Fe,Nb)_xO_3 ? δ (x = 0.05, 0.10) perovskite oxides were synthesized by the solid-state method. Structural and chemical stability of the SrCo_1 ? 2x(Fe,Nb)_xO_3 ? δ (x = 0.05, 0.10) oxides were studied by differential scanning calorimetry (DSC), thermogravimetric analysis (TG) and X-ray diffraction (XRD). The results demonstrated that the structural and chemical stability of the Fe/Nb co-doped SrCo_1 ? 2x(Fe,Nb)_xO_3 ? δ (x = 0.05, 0.10) is improved significantly. The oxygen sorption properties of the SrCo_1 ? 2x(Fe,Nb)_xO_3 ? δ (x = 0.05, 0.10) oxides were investigated between 300–900 °C in air, and the high oxygen sorption capacity of 11.5 and 10.3 mL O₂ (STP)/g oxide, respectively, are obtained.     

Silica nanoparticles with enlarged nanopore size for the loading and release of biological proteins

Silica nanoparticles (SNs) with a nanoporous structure are attractive for the delivery of biomolecules. This study developed a SNs-based protein delivery system with nanopore sizes large enough to uptake protein molecules. The use of trioctylmethylammonium bromide (TOMAB) as an auxiliary chemical facilitated a dramatic increase in pore size from 2.6 nm to 17.4 nm. The surface was highly negatively-charged with a zeta potential of approximately ? 35 at pH 7. Positively-charged protein cytochrome C was encapsulated effectively within the large pore spaces of the SNs, with a protein loading capacity of almost 2-fold increase due to the pore size increase. The loaded protein exhibited sustained release for approximately one week with an initial burst in a day, suggesting the SNs tailored with enlarged nanopores should be useful for the delivery of large protein molecules for tissue regeneration.     

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.     

Thermoreversible behavior of κ-carrageenan and its apatite-forming ability in simulated body fluid

Osteoconductive materials with self-setting ability have received much attention because their properties allow developing injectable materials for bone defects. Thermosensitive hydrogel with ability of bone-like apatite formation in a body environment is a candidate of injectable bone fillers with osteoconductivity because the apatite formation on materials is an essential to show osteoconduction. The present study focused on the development of a thermosensitive hydrogel through modifications of the sulphonic groups of the polysaccharide, κ-carrageenan, with potassium chloride (KCl) and calcium chloride (CaCl₂). We found that the gelation temperature of κ-carrageenan solutions increased with increasing amounts of K⁺ ions. Apatite formation was observed on the gel after exposure to simulated body fluid for 0.5 day when the gel was prepared with a molar ratio of Ca²⁺/sulfonic groups = 1.5. These results indicate that a thermosensitive κ-carrageenan hydrogel with apatite-forming ability was obtained through the incorporation of K⁺ and Ca²⁺ ions into the solution.     

Studies on melt spinning. VII. Elongational viscosity and fiber morphology of multiphase polymer systems

Melt spinning experiments were carried out to investigate the elongational behavior and fiber morphology of multiphase polymer systems. Materials chosen for study were blends of calcium carbonate-filled polypropylene with general-purpose polystyrene and blends of calcium carbonate-filled polypropylene with high-impact polystyrene. The former is a three-phase system in which the CaCO₃ particles are dispersed, and the latter is a four-phase system in which CaCO₃ particles are dispersed, together with rubbery butadiene particles. Note that polypropylene is incompatible with the matrix of high-impact polystyrene. The experimental technique described in part I of this series was used to determine the elongational viscosity. With the four-phase system, the apparent elongational viscosity tends to increase as the stretch ratio is increased above a certain critical value which appears to be ca. 25. This transition does not occur with the three-phase system and is attributable to elongation of the suspended rubber particles. The addition of small amounts of HIPS to PP-CaCO₃ increases spinnability in general, whereas larger amounts decrease spinnability.     

Wet oxidation of wastewater containing hydrocarbons by novel supported Pd catalysts

Pd catalysts supported on TiO₂, ZrO₂, ZSM-5, MCM-41 and activated carbon were used in catalytic wet oxidation of hydrocarbons such as phenol, m-cresol and m-xylene. It was found that the Pd/TiO₂ catalyst was highly effective in the wet oxidation of hydrocarbon. The activities of catalysts with various hydrocarbon species, catalyst support, oxidation state of catalyst performed in a 3-phase slurry reactor show that reaction on Pd surface is more favorable than that in aqueous phase and that the active site is oxidized Pd in catalytic wet air oxidation of hydrocarbons. Based on the experimental results, a plausible reaction mechanism of wet oxidation of hydrocarbons catalyzed over Pd/TiO₂ catalyst was proposed. This catalyst is superior to other oxide catalysts because it suppressed the formation of hardly-degradable organic intermediates and polymer.