Monodisperse polymer/metal composite particles by electroless chemical deposition: Effect of surface functionality of polymer particles

Micron‐sized polymer particles were coated with layers of nickel compounds by plating electrolessly in the presence of aqueous solutions of nickel chloride, sodium hypophosphite, sodium citrate, and ammonium chloride at elevated temperature. The uniform functional polymer particle could be obtained by seeded polymerization. To investigate the effect of surface functionality on the conditions for nickel deposition, the polymer particle was functionalized with the thiol group. From morphological observation, it was found that the mode of nickel deposition was greatly dependent on the surface functionality of the polymer particle. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 420–424, 2003     

Item recommendation based on context-aware model for personalized u-healthcare service

A personalized service in the ubiquitous environment is to provide services or items, which reflect personal tastes, attitudes, and contexts. It is impossible to reflect the context information generated in u-healthcare environments due to the existing recommendation system performing the recommendation using the information directly input by users and application usage record only. This study develops a context-aware model using the context information provided by the context information model. The study applies it to the extraction of the missing value in a collaborative filtering process. The context-aware model reflects the information that selects items by users according to the appropriate context using the C-HMM and provides it to users. The solution of the missing value in the preference significantly affects the recommendation accuracy in a preference based item supply method. Thus, this study developed a new collaborative filtering for ubiquitous environments by reflecting the missing preference value and reflecting it to the collaborative filtering using the context-aware model. Also, the validity of this method will be evaluated by applying it to menu services in u-healthcare services.     

Cure kinetics of epoxy formulations of the type used in advanced composites

An analysis of the cure kinetics of three different formulations composed of tetraglycidyl 4,4′-diaminodiphenyl methane (TGDDM) epoxy resin and diaminodiphenyl sulfone (DDS) was performed. A series of isothermal tests was run, and the experimentally obtained results were checked against the proposed kinetic model. An autocatalyzed mechanism with the overall reaction order of 2 was found to adequately describe the cure kinetics. An increase in reaction rate was observed at higher temperature and higher DDS concentration. For a given formulation, the extent of reaction corresponding to the maximum reaction rate was independent of temperature. A secondary exotherm was detected, particularly in formulations with low DDS concentration, at approximately 40% conversion. At that point, the rate of primary amine–epoxide reaction decreases, and other reactions dominate the curing process. Such a mechanism is likely to cause a formation of an inhomogeneous thermoset morphology.     

Strain-Induced Deformation in Magnesia–Alumina Layered Composites

Ceramic beams are induced in situ to form complex shapes at elevated temperature without the application of an external stress. This process has been demonstrated for thin alumina substrates coated with a layer of magnesia. The internal strain causing the substrates to deform at elevated temperature arises as a consequence of strain mismatch accompanying the penetration of the coating into the substrate. The magnitude of the deformation depends on the amount of coating applied, on the thickness of the substrate, on the density of the substrate, and on the temperature. During exposure of the beams to elevated temperature, the magnesia coating reacts with the alumina substrate to form the spinel phase; the resulting volume change accompanying the phase transformation is likely the predominant driving force for deformation.     

Preparation of phenolic resin derived 3-D ordered macroporous carbon

Three-dimensionally ordered long-range macroporous carbon structures were prepared using commercially available phenolic resin by utilizing sacrificial colloidal silica crystalline arrays as templates that were subsequently removed by HF etching after pyrolysis in an argon atmosphere. SEM, TEM, and BET were employed to characterize the morphology and the surface area of the porous carbon structures. The pore size (150–1000 nm) and BET surface area, which reflect pore volume (298.6 m²/g (1.32 cm³/g) ∼ 93.7 m²/g (0.12 cm³/g)), of the macroporous carbon structures produced were approximately proportional to the size (150–1000 nm) of the sacrificial silica sphere templates used (annealing temp. 550°C). The achieved 550 nm porous carbon structures were examined to function as potential catalyst carriers and were successfully impregnated with Ag or Pt-Ru on their inner walls after borohydride reduction at room temperature. In addition, porous carbon patterns were fabricated using the ‘micromolding in capillary’ technique, which has potential applications in the microreaction technology.     

A study on the factors for improving the ethanol production from Jerusalem artichoke by Kluyveromyces fragilis

This study is to investigate the factors influencing the alcohol production byKluyveromyces fragilis using the juice of Jerusalem Artichoke tubers. The cell growth rate and ethanol production rate were stimulated by aeration and by the addition of unsaturated fatty acids and the cell mass production and the ethanol production were substantially improved. It was found that oxygen and unsaturated fatty acids added played a decisive role on the increase of alcohol tolerance of yeast.     

Synthesis of biodegradable PU/PEGDA IPNs having micro-separated morphology for enhanced blood compatibility

Summary New biodegradable hydrophobic polyurethane (PU)/hydrophilic poly (ethylene glycol) diacrylate (PEGDA) IPN was simultaneously synthesized with changing the molecular weight of PEGDA to investigate the effect of crosslinking density on the degree of phase separation. PU was modified using biodegradable poly(-caprolactone)diol and the hydroxy group of PEG was substituted to crosslinkable acrylate group having double bond, which induce photo-polymerization. The sturucture of PEGDA was confirmed by NMR. Because the reaction rate of PEGDA was faster than that of PU, the continuous matrix of the micro-separated PU/PEGDA IPNs having amphiphilic character was made of hydrophilic PEGDA-rich phase. All IPNs have sea-island morphology resulting from the suppressed phase separation. The effect of the degree of phase separation on blood compatibility was investigated.     

Dissipative structures of autocatalytic reactions in tubular flow reactors

Dissipative structures of autocatalytic reactions with initially uniform concentrations are studied in tubular flow reactors. A unique steady state exists in a continuous stirred tank reactor. Linear stability analysis predicts either a stable node, a focus or an unstable saddle-focus. Sustained oscillations around the unstable focus can occur for high values of Damköhler number. In distributed parameter systems, travelling, standing or complex oscillatory waves are detected. For low values of Damköhler number, travelling waves with pseudo-constant patterns are observed. With intermediate values of Damköhler number, single or multiple standing waves are obtained. The temporal behavior indicates also the appearance of retriggering or echo waves. For high values of Damköhler number, both single peak and complex multipeak oscillations are found. In the cell model, both regular oscillations near the inlet and chaotic behavior downstream are observed. In the dispersion model, higher Peclet numbers eliminate the oscillations. The spatial profile shows a train of pulsating waves for the discret model and a single pulsating or solitary wave for the continuous model.     

Oxidation Behavior and Flexural Strength of Aluminum Nitride Exposed to Air at Elevated Temperatures

The oxidation behavior of a sintered aluminum nitride containing 3 wt% Y₂O₃ as a sintering aid was investigated. Samples were exposed to air at elevated temperatures for times up to 100 h. The weights of the samples were continuously monitored during exposure at various temperatures and humidity levels. The effects of oxidation on room-temperature flexural strength were also determined, and correlated to the observed weight changes of the samples. At temperatures 1200°C, linear weight gains were observed. However, at temperatures above 1200°C, the weight gains became parabolic with respect to exposure time. The oxidation rates were significantly increased by water vapor in the air. The oxidation products were found by X-ray analysis to be a mixture of Al₂O₃ and 5A1₂O₃·3Y₂O₃. The oxide layer formed on the surface was severely cracked because of the thermal expansion mismatch between the oxide layer and the substrate. The cracks initiated in the oxide layer and propagated into the substrate, resulting in severe reduction in the room-temperature flexural strength of the material. When exposed to ambient air for more than 50 h at temperatures greater than 1100°C, the strengths of the samples decreased to less than half that of the as-received material.     

Spinning viscose technical yarn into a bicomponent precipitation bath

Conclusions -- The possibility has been demonstrated of preparing viscose yarn by the centrifugal method from a viscose containing additions of urea by spinning into a bicomponent precipitation bath containing sulfuric acid and sodium sulfate.-- Optimum conditions for spinning viscose yarn have been established: a sulfuric acid content of 115 g/l in the precipitation bath, a urea content of 2.5% based on weight of -cellulose in the viscose, and an orientation stretch of 22%.-- Specimens of viscose yarn having a linear density of 13.3 tex have been prepared with a relative breaking load of up to 19 cN/tex, an elongation at break of 17–19%, and a mean squared deviation in dyeing nonuniformity of 0.8–1.0.Translated from Khimicheskie Volokna, No. 4, pp. 33–34, July–August, 1990.