Long-Term Deterioration of GFRP in Water and Moist Environment

This report examines the effects of water and moisture on the durability of pultruded glass-fiber-reinforced polymers (GFRP) with vinylester resin for applications in normal air conditions. Deterioration tests, including both immersion and atmosphere conditions at various temperatures, were conducted to investigate the deterioration characteristics of pultruded GFRP after being permeated by water. The main findings from the tests were that cracks appeared on the surface of the GFRP and that the weight of the materials decreased, which may be attributed in the surface treatment oil for the glass-fiber cloth being dissolved away. The bending strength of the GFRP was also found to be reduced. The rate of weight decrease and the reductions in bending strength were greater in a 60°C water-immersion condition compared to both a 60°C moist-atmosphere condition and a 40°C water-immersion condition. This difference is due to the fact that the glass fiber and matrix resin separated in water at 60°C. Although the matrix resin changed color in air at 60°C, becoming noticeably brown, no chemical changes were found by infrared spectra.     

Preparation and rate capability of Li4Ti5O12 hollow-sphere anode material

Spinel lithium titanate, Li₄Ti₅O₁₂, with novel hollow-sphere structure was fabricated by a sol–gel process using carbon sphere as template. The effect of the hollow-sphere structure as well as the wall thickness on the Li storage capability and high rate performance was electrochemically evaluated. High specific capacity, especially better high rate performance was achieved with this Li₄Ti₅O₁₂ hollow-sphere electrode material with thin wall thickness. It is believed that this macroporous hollow-sphere structure has shortened the Li diffusion distance, increased the contact area between Li₄Ti₅O₁₂ and electrolyte, and also led to better mixing of the active material with AB. All these factors have resulted in the good rate capability of the hollow-sphere structured Li₄Ti₅O₁₂ electrode material.     

Sugar-Induced Chiral Orientation of Boronic-Acid-Appended Amphiphile Clusters Formed in the Dipalmitoylphosphatidylcholine (DPPC) Membrane

A boronic-acid-appended amphiphile bearing an azobenzene chromophore in the chain center ( 3 ) was synthesized. Although 3 could not form the membrane-like, ordered aggregate by itself, it formed a phase-separated aggregate in a dipalmitoylphosphatidylcholine (DPPC) matrix membrane. When saccharides were added, the boronic acid group reversibly formed the saccharide complexes, and 3 in the DPPC matrix membrane became CD-active with the appearance of exciton-coupling bands. Comparison of the saccharide absolute configuration with the CD intensity established that the saccharide possessing the OH group (as 3-OH, 4-OH, and 5-CH₂OH) in the same side as the cis-1,2-diol gives the strong CD band. Judging from the structure of 3 –saccharide complexes, these “same-side” OH groups can enjoy intermolecular hydrogen-bonding interactions, which eventually induce the chiral orientation of azobenzene chromophores. This is a novel membrane system useful to read out the information stored in the saccharide structure and to create novel membrane structures by added saccharides.     

Calculation of the interfacial properties of liquid steel – slag systems

The rates of many high temperature metallurgical reactions are strongly influenced by interfacial phenomena and to determine reaction rates it is necessary to have an accurate model of interfacial properties. In this article, the factors governing interfacial tension in slag-metal systems will be briefly discussed and, a model based on the combination of the Gibbs and Langmuir adsorption isotherms with Girifalco and Good's expression for the interfacial tension between immiscible liquids, will be shown to be consistent with current literature values and allow the calculation of both the interfacial tension and the contact angle between liquid slags and liquid iron in the CaO–CaF₂–SiO₂–Al₂O₃ system. The application of this approach to systems containing FeO in the slag and carbon in the metal are then discussed.     

Nicotinic receptors are regulated by protein kinase C activated via a nicotinic receptors-mediated signaling pathway

Previously we reported than BO-IMI, a reagent which contains a BODIPY fluorophore linked to an imidazole group, can be used to covalently label a phosphomonoester in a single step under aqueous conditions [P. Wang, R.W. Giese, Anal. Chem. 65 (1993) 3518]. The reaction was conducted in the presence of a water-soluble carbodiimide 1-ethyl-3-(3'-N,N'-dimethylaminopropyl) carbodiimide [EDC] to activate the phosphomonoester, and the coupling took place onto both the N1 and N3 imidazole nitrogens of BO-IMI. Whether the two BO-IMI-phosphomonoester regioisomers migrated separately or together during capillary electrophoresis depended on the pH, due to a difference in their pKa values. Since then, we have studied the reaction in more detail leading to the information reported here. First, we have learned that the regioisomer ratio changes during the course of the reaction, and found that the mechanism involves both spontaneous and BO-IMI-catalyzed hydrolysis of the less stable isomer. Second, there is a background reaction in which BO-IMI becomes attached to EDC. Third, the BO-IMI-phosphomonoester product (a mixture of two isomers), that is observed by capillary electrophoresis at an alkaline pH, is found to no longer contain the two fluorine atoms present in the starting BO-IMI reagent. This is because they are placed by hydroxy groups at high pH. Finally, an event was discovered which complicates the detection of less than about 60 fmol of a phosphomonoester with BO-IMI: hydrolysis of a tiny fraction of the BO-IMI takes place during the coupling reaction, which leads to chemical noise in the capillary electropherogram.     

The dispersion of a sound velocity near the phase transition point of csd2PO4

The relaxation time τ of the polarization fluctuation is obtained from the frequency dependence of the sound velocity in MHz region. The value of τ is the order of 10 nsec just below the phase transition point and agrees with that obtained from the dispersion of the dielectric constant.     

Chemical gas sensor application of open-pore mesoporous thin films based on integrated optical polarimetric interferometry

Chemical gas sensors that employ integrated optical polarimetric interferometry were fabricated by the sol-gel synthesis of transparent mesoporous thin films of TiO2-P2O5 nanocomposite on tapered layers of TiO2 sputtered on tin-diffused glass waveguides. Atomic force microscopy images of the mesoporous thin film clearly show the open pore mouths on the film surface that favor rapid diffusion and adsorption of gas-phase analytes within the entire film. Adsorption of gas and vapor induces changes (Deltan) in the refractive index of the mesoporous thin film that lead to shifts in the phase difference between the fundamental transverse electric and magnetic modes simultaneously excited in the glass waveguide via single-beam incidence. Upon exposure to NH3 gas at concentrations as low as 100 ppb in dry air at room temperature, the sensor exhibits a reversible change in the phase difference with the response and recovery times of less than 60 and 90 s, respectively. It is unexpected that the sensor is unresponsive to either NO2 or C6H6 vapor, leading to a somewhat selective sensitivity to NH3. Determination of Deltan was carried out with a combination of the experimental results and the theoretical calculations. The sensor design represents a novel, effective, and easily accessible approach to mesoporous thin-film-based integrated optical chemical sensors.