Free-standing single-walled carbon nanotube/SnO2 anode paper for flexible lithium-ion batteries

Free-standing single-walled carbon nanotube/SnO₂ (SWCNT/SnO₂) anode paper was prepared by vacuum filtration of SWCNT/SnO₂ hybrid material which was synthesized by the polyol method. From field emission scanning electron microscopy and transmission electron microscopy, the CNTs form a three-dimensional nanoporous network, in which ultra-fine SnO₂ nanoparticles, which had crystallite sizes of less than 5 nm, were distributed, predominately as groups of nanoparticles on the surfaces of single walled CNT bundles. Electrochemical measurements demonstrated that the anode paper with 34 wt.% SnO₂ had excellent cyclic retention, with the high specific capacity of 454 mAh g^?1 beyond 100 cycles at a current density of 25 mA g^?1, much higher than that of the corresponding pristine CNT paper. The SWCNTs could act as a flexible mechanical support for strain release, offering an efficient electrically conducting channel, while the nanosized SnO₂ provides the high capacity. The SWCNT/SnO₂ flexible electrodes can be bent to extremely small radii of curvature and still function well, despite a marginal decrease in the conductivity of the cell. The electrochemical response is maintained in the initial and further cycling process. Such capabilities demonstrate that this model hold great promise for applications requiring flexible and bendable Li-ion batteries.     

Microwave sintering and grain growth behavior of nano-grained BaTiO3 materials

In this paper, we investigated the effect of microwave sintering parameters on the development of the microstructure of nano-grained BaTiO₃ materials co-doped with Y and Mg species. It is observed that the materials can not only be sintered densely at a lower temperature (1150 °C) and a shorter soaking time (20 min), but also the grain growth can be suppressed by 2.45 GHz microwave heating process. However, the grain growth exhibits a unique tendency in some processing conditions such as microwave sintering for longer intervals (≧60 min) or at higher temperatures (1200 °C). The grain growth behavior after densification was investigated in terms of the phenomenological kinetics, and the activation energy for grain growth using microwave sintering (59.4 kJ/mol) is considerably less than that of the conventionally sintered ones (96.0 kJ/mol), which indicates that microwave sintering process can accelerate the densification rate of the BaTiO₃ materials comparing with the conventional sintering process.     

Protective Effect of Caffeic Acid on Paclitaxel Induced Anti-Proliferation and Apoptosis of Lung Cancer Cells Involves NF-κB Pathway

Caffeic acid (CA), a natural phenolic compound, is abundant in medicinal plants. CA possesses multiple biological effects such as anti-bacterial and anti-cancer growth. CA was also reported to induce fore stomach and kidney tumors in a mouse model. Here we used two human lung cancer cell lines, A549 and H1299, to clarify the role of CA in cancer cell proliferation. The growth assay showed that CA moderately promoted the proliferation of the lung cancer cells. Furthermore, pre-treatment of CA rescues the proliferation inhibition induced by a sub-IC(50) dose of paclitaxel (PTX), an anticancer drug. Western blot showed that CA up-regulated the pro-survival proteins survivin and Bcl-2, the down-stream targets of NF-κB. This is consistent with the observation that CA induced nuclear translocation of NF-κB p65. Our study suggested that the pro-survival effect of CA on PTX-treated lung cancer cells is mediated through a NF-κB signaling pathway. This may provide mechanistic insights into the chemoresistance of cancer calls.     

Effects of the organometallic coupling agents on adhesion of the carbon fiber–BMI composites

In order to increase the chemical bonding force between fiber and resin, several kinds of organometallic coupling agent (such as titanate, zirconate, and zircoaluminate) were chosen and added in the BMI resin formulation, which possess the same solvent system with those coupling agents. The DSC analysis technique was used to find the best curing condition, and TGA was used to investigate the thermal stability property of the best curing condition. For the purpose of analyzing the bonding structure, ESCA surface element analysis techniques was applied in this study. Beside that, the mechanical properties of tensile, flexural, and short-beam shear strengths were measured for the effect of adding coupling agents, and the SEM of fracture surfaces were taken to study the fractural analysis. The results showed that composites with the application of organometallic coupling agents of [RO–Ti(OX–R′NH₂)₃] structure in the treatment of BMI resin were highly thermal stable. Also, it was shown that the mechanical strengths of composites fabricated by pretreatment of the carbon fibers with coupling agents were higher than those fabricated by adding coupling agents in resins, but there was no obvious improvement of mechanical properties with higher concentration of coupling agents. However, the SEM showed that the adhesion between fiber and resin can actually be improved by adding proper amount of coupling agents in the BMI resin formulation.     

Paired electrooxidation IV. Decarboxylation of sodium gluconate to D-arabinose

A paired electrooxidative method has been developed to synthesize D-arabinose in a divided cell. D-arabinose is a material which has an important role in the production of vitamin B2 and DNA. Sodium gluconate was directly oxidized at the anode and indirectly oxidized in the catholyte by bubbling oxygen which was reduced to H₂O₂ and OH free radicals. In the catholyte, indirect oxidation of sodium gluconate was mediated by Fe³⁺ and OH free radicals. The optimal current efficiencies for D-arabinose production in the anolyte and catholyte were found to be 88.37% and 39.12%, respectively, and the total current efficiency of the paired electrooxidation was 127.49%. The paired electrosynthesis of D-arabinose is more economical in terms of power consumption than electrosynthesis that employ a single anode or cathode as the working electrode. The influence of cathodic/anodic CV and I/E curves, redox mediators and the amount of charge passed were also examined.     

Gas-Phase Catalysis by Micelle Derived Au Nanoparticles on Oxide Supports

The reactivity of gold clusters (8–22 nm diameter) supported on different metal oxides (titanium dioxide (TiO₂), zinc oxide (ZnO), zirconium oxide (ZrO₂), and silicon dioxide (SiO₂)) was investigated in a continuous flow reactor. Clusters were encapsulated within polymer in toluene solution, impregnated onto the bulk supports, and reduced by calcination at 300 °C. Support dependent sintering (TiO₂>ZrO₂>ZnO) was observed following heating in air at 300 °C. For both CO oxidation and propylene hydrogenation, Au nanoclusters on TiO₂ exhibit the highest activity compared to other supports.     

Preparation of fluoroacrylate nanocopolymer by miniemulsion polymerization used in textile finishing

Latex based on fluoroacrylate (TAN) and other comonomers was prepared via miniemulsion polymerization in the presence of stearyl trimethyl ammonium chloride (STAC) and 2, 2′‐azobis (2‐amidinopropane) dihydrochloride (ABAP) as a water soluble initiator. Light transmittance studies demonstrated that the light transmittance of prepared emulsions increases with the amount of TAN, STAC, cosolvent DPM, and hydrophobe DM. Given suitable reaction temperature and quantities of TAN, STAC, DPM, and DM, a copolymer emulsion of fluoroacylate with a particle size of 50 nm was produced. The water repellency tested on polyester fabrics displayed greater effectiveness than that of commercial products with higher fluorine content. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1466–1472, 2004     

Effect of Microstructure of ZnO Nanorod Film on Humidity Sensing

In this study, a simple thick‐film humidity sensor was fabricated by coating wet‐synthesized ZnO nanorods on screen‐printing interdigitated electrodes. We investigated the influence of the coating procedure on the microstructure of ZnO nanorod films and thereby on humidity sensing. The experimental results revealed that the specific surface area (SSA) decreased and the average pore size (APS) increased with increasing the sintering time and the number of coating layer. The humidity response depended significantly on the pore properties of the ZnO nanorod films. By virtue of the incipient wetness analysis, it was found that the adsorption of water molecules on the ZnO surface led to the decrease in electrical resistance even though the ZnO was rod like, n‐type semiconductor. While tuning the pore structure of the ZnO nanorod film, the thick‐film humidity sensor might display near‐linear response in the full range of 0%–100% relative humidity (RH).     

New Perspectives on the Gas–Solid Reaction of α‐Si3N4 Powder in Wet Air at High Temperature

The reaction behavior of chemically vapor‐deposited silicon nitride (α‐Si₃N₄) powder in wet air at 1673–1873 K for 10 h has been investigated. The oxidation and volatilization reaction coexist initially while volatilization reaction progressively becomes the limiting step with extended reaction time. Based on the experimental curves, a new kinetic model regarding both solid product layer and hypothetically volatile product layer has been developed to interpret its short‐term reaction and predict long‐term corrosion behavior. The calculated results agree well with the experimental data. Predictably, this new kinetic model can not only be used to treat the reaction of Si₃N₄ powder in wet air but also can be applied to deal with the gas–solid reaction of other ceramic powders.     

Humic Substances Affect the Activity of Chlorophyllase

Three humic substances--humic acid, fulvic acid, and humin--were isolated from soils located in the northern and southern forests of the Yuanyang Lake Nature Preserve in northern Taiwan's Ilan County. Aqueous extracts of fresh wet soil and of three humic substances, at concentrations of 0.125, 0.25, and 0.5 mg/ml, were investigated for their effects on the activities of chlorophyllase a and b. Aqueous extracts of forest soils at the northern and southern bank, dominated by the pure vegetation of Formosan False cypress (Chamcaecyparis formosensis Matsum), stimulate both chlorophyllase a and b activities, while those of the southern bank, dominated by a Taiwanese Miscanthus (Miscanthus transmorrisonensis Hayata), inhibits such activities. All three humic substances, despite their soil sources, stimulate the activities of both chlorophyllase a and b. Fulvic acid stimulates more chlorophyllase a activity than either humic acid or humin. Humic acid stimulates more activity of chlorophyllase b than either fulvic acid or humin. Humin exhibited the least effect on chlorophyllase a and b. It is suggested that humic substances in the soil may accelerate the chlorophyll degradation of litter in the ecosystem and that chlorophyllase a and b may be different enzymes.