Preparation and gas permeation of immobilized fullerene membranes

Fullerene‐dispersed membranes were homogeneously prepared under the conditions in which a 10 wt % polystyrene solution containing 1 wt % fullerene was dried under a reduced pressure of 50 cmHg at room temperature. The fullerene membranes prepared with 1,2‐dichlorobenzene were found to have the darkest color, and showed no evidence of fullerene crystals in their photomicrographs. UV‐visible and infrared absorption spectra of the fullerene membranes showed fullerene bands, which indicated that the fullerene was homogeneously dispersed in the membranes. The permeability coefficients of pure nitrogen, oxygen, carbon dioxide, ethane, and ethylene were found to increase significantly in the fullerene membranes compared to those in the polystyrene membranes, although the ideal separation factors for oxygen/nitrogen and ethylene/ethane in the fullerene membranes (i.e., 4.3 and 1.7, respectively) were slightly less than the separation factors in the polystyrene membranes. The permeability increase originated from the increase in diffusion coefficients in the fullerene membranes. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 529–537, 2000     

Bounding Surface Model for Geosynthetic Reinforcements

Geosynthetic reinforcements are manufactured from polymers such as polyester, polypropylene, and high-density polyethylene. Compared to metals, they exhibit large plastic strains, and highly nonlinear and hysteretic behaviors under cyclic loading. Most geosynthetic reinforcements do not sustain compression load. Traditional cyclic models with the Masing rule fail to simulate such unique behavior. A 1D bounding surface concept is used to develop a model that considers these unique properties of geogrids. The unique features of the model include nonparallel bounding lines and different loading and unloading hardening parameters. The model was calibrated and compared with the experimental results of two geogrids under monotonic and cyclic loadings with different load amplitudes.     

Incorporation of transition metal in porous glass-ceramics of TiO2-SiO2 system

Incorporation of transition metals in porous glass-ceramics of TiO₂-SiO₂ system was made by the phase separation and crystallization of the glasses of TiO₂-SiO₂-Al₂O₃-P₂O₅-CaO-MgO system containing various kinds of transition metals. The amount of transition metals incorporated in the skeleton of the porous glass-ceramics was dependent on both chemical composition of mother glass and conditions of heat treatment. In general the amount decreased with the increasing amount of rutile in the skeleton. In the glass of high TiO₂/SiO₂ ratio, the incorporation of relatively large amounts of transition metals was possible even if the precipitation of a fairly large amount of rutile occurred. The crystallization of rutile and in porous glass-ceramics was essential to fabricate rigid platelet porous glass-ceramics.     

Multiple stack performance near saturation

Detailed simulation experiments have been performed to study multiple stack performance, primarily using two methods recently developed by the authors called dynamic initial allocation and local reallocation procedures. Some results are: determining first occurrences of overflows in terms of storage saturation; observing performance behaviours, particularly for near full storage saturation; and performance evaluation on the weight of two storage redistribution schemes, one being based on the most recent stack growth, the other on the current stack size. Also discussed is the issue of whether additional space should be sought when storage is near saturation, and if so, how it is to be obtained. The critical stack saturation percentage is proposed as the point where additional storage space should be sought. It is the one at which the expected total cost is the minimum.     

Crystallization behaviour and hardness of glass ceramics rich in nanocrystals of ZrO2

This research is mainly directed toward the development of hardness of glass ceramic by adding different amounts of ZrO₂ to the glass and by applying different heat-treatments. Differential thermal analysis (DTA), X-ray diffraction (XRD) and Scanning electron microscope (SEM) were used to study the crystallization behaviour of the glass samples. The only observed crystalline phases were tetragonal and monoclinic zirconia. Hardness was found to increase by increasing time and temperature of heat-treatment due to the formation of monoclinic phase as a result of the martensitic reaction. This transformation opposes crack opening.     

Permeation properties of hydrogen and water vapor through porous silica membranes at high temperatures

Silica and cobalt‐doped silica membranes that showed a high permeance of 1.8 × 10^?7 mol m^?2 s^?1 Pa^?1 and a H₂/N₂ permeance ratio of ～730, with excellent hydrothermal stability under steam pressure of 300 kPa, were successfully prepared. The permeation mechanism of gas molecules, focusing particularly on hydrogen and water vapor, was investigated in the 300–500°C range and is discussed based on the activation energy of permeation and the selectivity of gaseous molecules. The activation energy of H₂ permeation correlated well with the permeance ratio of He/H₂ for porous silica membranes prepared by sol–gel processing, chemical vapor deposition (CVD), and vitreous glasses, indicating that similar amorphous silica network structures were formed. The permeance ratios of H₂/H₂O were found to range from 5 to 40, that is, hydrogen (kinetic diameter: 0.289 nm) was always more permeable than water (0.265 nm). © 2010 American Institute of Chemical Engineers AIChE J, 2011     

The embrittlement mechanism and improvement of impact strength for lead-free solder joints in BGA packaging using electrolytic Ni/Au plating

Impact strength evaluation and fracture mechanism analysis in board level of Sn–3mass%Ag–0.5mass%Cu solder joints of ball grid arrays (BGA) using electrolytic Ni/Au plating were performed. The cause of impact strength degradation of BGA solder ball joints is the existence of low density defects, which contain organic materials, in the (Cu,Ni)₆Sn₅ intermetallic compound grain boundary formed in the solder joints. These organic materials are taken in by the nickel plating film at the time of nickel plating. To improve the impact strength of the Sn–3mass%Ag–0.5mass%Cu solder joint of the BGA, it is necessary to lower the concentration of these organic materials. The contamination prevention and nickel plating bath sanitization, solder mask material selection (to minimize nickel plating bath contamination) and higher current density of nickel plating are effective to keep a lower concentration of organic materials in nickel plating film.     

Seismic performance of small earth dams with sloping core zones and geosynthetic clay liners using full-scale shaking table tests

In Japan, a large number of old small earth dams are in critical need of repair due to leakage and poor earthquake resistance. In addition to cohesive soils, geosynthetic clay liners (GCLs) are used as impervious materials to repair such dams. This paper discusses the seismic performance of small earth dams, with reservoirs on their upstream side, repaired with a sloping core zone and a GCL on the basis of the results of full-scale shaking table tests performed at the E-Defense facility. The main focus is on the differences in mechanical behavior between the upstream and downstream sides of the dam. The results elucidate that the effective stress of the upstream embankment materials increased because of the undrained shear behavior of the compacted soils, although the deformation on the upstream side was larger than that on the downstream side. A large phase difference in the measured accelerations between the upstream slope and the downstream slope was also observed. Therefore, it is concluded that significant differences occurred in the dynamic behavior of the upstream side and the downstream side.     

Enhancement of the actuation performance of dielectric triblock copolymers modified with additives

To enhance actuation performance without prestrain, an elastomeric acrylic triblock copolymer, poly(methyl methacrylate)‐block‐poly(n‐butyl acrylate)‐block‐poly(methyl methacrylate), was modified with two kinds of additives, oligomeric poly(n‐butyl acrylate) and the plasticizer dibutyl sebacate. An actuator modified with those additives showed about 6% strain, whereas the unmodified actuator showed only 1% strain for the same applied electric field without prestrain. In addition, actuation was attained at lower critical electric field strength (625 and 1000 V mm^?1 for modified and unmodified actuators, respectively). Upon increasing the amounts of the additives, the electrically induced actuation velocity and degree of deformation increased. These results are explained by the dielectric and mechanical properties of the elastomers. The dielectric constants for elastomers modified with dibutyl sebacate were larger than those for elastomers modified with oligomeric poly(n‐butyl acrylate). The initial tensile stresses of both of the modified elastomers were much smaller than that of unmodified elastomer. The results provide a route to enhancing actuation performance of dielectric elastomers without prestrain. Copyright © 2011 Society of Chemical Industry     

Hydrogen Permeation Properties and Hydrothermal Stability of Sol–Gel‐Derived Amorphous Silica Membranes Fabricated at High Temperatures

The sol–gel method was applied to the fabrication of amorphous silica membranes for use in hydrogen separation at high temperatures. The effects of fabrication temperature on the hydrogen permeation properties and the hydrothermal stability of amorphous silica membranes were evaluated. A thin continuous silica separation layer (thickness = <300 nm) was successfully formed on the top of a deposited colloidal silica layer in a porous glass support. After heat treatment at 800°C for an amorphous silica membrane fabricated at 550°C, however, it was quite difficult to distinguish the active separation layer from the deposited colloidal silica layer in a porous glass support, due to the adhesion of colloidal silica caused by sintering at high temperatures. The amorphous silica membranes fabricated at 700°C were relatively stable under steam atmosphere (500°C, steam = 70 kPa), and showed steady He and H₂ permeance values of 4.0 × 10^?7 and 1.0 × 10^?7 mol·m^?2·s^?1·Pa^?1 with H₂/CH₄ and H₂/H₂O permeance ratios of ~110 and 22, respectively. The permeance ratios of H₂/H₂O for membranes fired at 700°C increased drastically over the range of He/H₂ permeance ratios by factors of ~3–4, and showed a value of ~30, which was higher than those fired at 500°C. Less permeation of water vapor through amorphous silica membranes fabricated at high temperatures can be ascribed to the dense amorphous silica structure caused by the condensation reaction of silanol groups.