Characteristics of interfacial profiles in upward and downward gas-liquid two-phase plug flow

Gas-liquid interfacial profiles in plug flow for both upward and downward flows were obtained using semi-supermultiple point-electrode probes, comprising 67 sensing tips arranged on a tube diameter. Typical interfacial profiles are demonstrated for both flows. Close inspection of the profiles reveals that four zones exist in a pair of gas and liquid slugs for upward plug flow and a high slip velocity region in downward plug flow. The lengths of the swelling liquid front zone and the wake zone were determined. The length of the wake zone strongly depends on the relative velocity between the liquid film around the gas slug and the liquid phase in the liquid slug. Characteristic distributions of bubbles within liquid slugs were found, i.e., three types of radial distributions of void fraction, namely saddle-shaped, trapezoidal and bullet-shaped distributions, exist for upward flow. The two types for downward flow exclude the saddle-shaped distribution. © 1997 Scripta Technica, Inc. Heat Trans Jpn Res, 25 (8): 568–579, 1996     

Pseudomonas aeruginosa as a model microorganism for investigation of chemotactic behaviors in ecosystem

Motile bacteria sense changes in the concentration of chemicals in environments and respond in a behavioral manner. This behavioral response is called chemotaxis. Bacterial chemotaxis can be viewed as an important prelude to metabolism, prey-predator relationships, symbiosis, infections, and other ecological interactions in biological communities. Genome analysis reveals that a large number of environmental motile bacteria possess a number of genes involved in chemosensing and chemotatic signal transduction. Pseudomonas aeruginosa has a very complex chemosensory system with more than 20 chemotaxis (che) genes in five distinct clusters and 26 chemoreceptor (methyl-accepting chemotaxis protein [mcp]) genes. Among the 26 MCPs of P. aeruginosa, nine have been identified as MCPs for amino acids, inorganic phosphate, oxygen, ethylene, and volatile chlorinated aliphatic hydrocarbons, whereas 3 MCPs were demonstrated to be involved in biofilm formation and biosynthesis of type IV pilus. Six che genes are essential for chemotactic responses, while genes in Pil-Chp cluster and Wsp cluster are involved in type IV pilus synthesis and twitching motility and biofilm formation, respectively. P. aeruginosa, with its complex chemotaxis system, is a better model microorganism for investigating ecological aspects of chemotaxis in environmental bacteria than Escherichia coli and Salmonella enterica serovar Typhimurium, which possess a relatively simpler chemotaxis system.     

Internal oxidation of Fe-Al alloys in the α-phase region

The internal oxidation behavior of Fe-0.069, 0.158, and 0.274 wt% Al alloys was investigated in the -phase region. The internal oxidation experiments have been made over the temperature range from 1023 to 1123 K using a mixture of iron and its oxide powders. A parabolic rate law holds in the present alloys, where the rate constant, K_p, depends upon the oxidation temperature as well as the aluminum content. The internal oxidation of Fe-Al alloys is, therefore, controlled by a diffusion process of oxygen in the alloy. The oxide formed in the oxidation layer is the stoichiometric FeAl₂O₄ (hercynite). The aluminum concentration, N _Al ^Io , in the oxidation layer was calculated by taking account of counterdiffusion of aluminum. Furthermore, the oxygen concentration, N _O ^S , at the specimen surface was evaluated on the basis of thermodynamics. Using these estimated values of K_p, N _Al ^IO , and N _O ^S , the diffusion coefficient of oxygen, D _O ^IO , in the oxidation layer, where the oxide particles were dispersed, was also calculated. D _O ^IO increases as the volume fraction of the oxide, f^IO, increases. The diffusion coefficient of oxygen, D_O, in -iron was determined by extrapolating D _O ^IO to f^IO=0.     

Evaluation of phosphate removal from water by immobilized phosphate-binding protein PstS

The phosphate (P(i))-binding protein PstS is a member of a family of periplasmic proteins that act as high-affinity receptors for active transport systems in bacteria. PstS protein purified from Pseudomonas aeruginosa was immobilized to N-hydroxysuccinimide-activated Sepharose, packed into a plastic column (5 x 70 mm), and examined for its potential ability to remove P(i) from water. The PstS-Sepharose column completely removed P(i) from 32P-labeled pond water containing about 0.5 microM P(i) (0.015 mg P per liter). More than 90% of 32P-P(i) that was retained in the column could be eluted by washing with low-pH water.     

Perovskite-type oxides La1−xSrxMnO3 for cathode catalysts in direct ethylene glycol alkaline fuel cells

Carbon-supported La_1−xSr_xMnO₃ (LSM/C) was prepared by reversible homogeneous precipitation method, and its catalytic activities for oxygen reduction under the existence of ethylene glycol (EG) were investigated by using rotating disk electrode. LSM/C exhibited the high activity for oxygen reduction irrespective with the presence of EG, indicating that EG is not oxidized by LSM/C at the cathode side in the present system. Consequently, LSM/C can serve as a cathode catalyst in alkaline direct alcohol fuel cells with no crossover problem. Performance test for fuel cells operation also supported these results and showed cathodic polarization curves were not affected by the concentration of EG supplied to anode even at 5 mol dm⁻³.     

Ordered Mesoporous Silica Derived from Layered Silicates

Here, the development of ordered mesoporous silica prepared by the reaction of layered silicates with organoammonium surfactants is reviewed. The specific features of mesoporous silica are discussed with relation to the probable formation mechanisms. The recent understanding of the unusual structural changes from the 2D structure to periodic 3D mesostructures is presented. The formation of mesophase silicates from layered silicates with single silicate sheets depends on combined factors including the reactivity of layered silicates, the presence of layered intermediates, the variation of the silicate sheets, and the assemblies of surfactant molecules in the interlayer spaces. FSM‐16‐type (p6mm) mesoporous silica is formed via layered intermediates composed of fragmented silicate sheets and alkyltrimethylammonium (C_nTMA) cations. KSW‐2‐type (c2mm) mesoporous silica can be prepared through the bending of the individual silicate sheets with intralayer and interlayer condensation. Although the structure of the silicate sheets changes during the reactions with C_nTMA cations in a complex manner, the structural units caused by kanemite in the frameworks are retained. Recent development of the structural design in the silicate framework is very important for obtaining KSW‐2‐based mesoporous silica with molecularly ordered frameworks. The structural units originating from layered silicates are chemically designed and structurally stabilized by direct silylation of as‐synthesized KSW‐2. Some proposed applications using these mesoporous silica are also summarized with some remarks on the uniqueness of the use of layered silicates by comparison with MCM‐type mesoporous silica.     

Properties of bifunctional phosphonate fibers derived from chloromethylstyrene grafted polyolefin fibers

Bifunctional fibers containing phosphonate and sulfonate were derived from chloromethylstyrene grafted polyolefin fibers (PPPE-g-CMS) by phosphorylation and subsequent sulfonation reactions. It was clarified that phosphorylation of PPPE-g-CMS by Arbusov reaction is more suitable than one by the reaction with PCl₃ in the presence of AlCl₃, because the latter damaged fibers and gave phosphinate groups in addition to phosphonate ones. Then, bifunctional fibers containing phosphonate and sulfonate groups were prepared by sulfonation of monofunctional phosphonate fibers obtained via Arbusov reaction with chlorosulfonic acid. The metal ion selectivity of the bifunctional fibers was governed by both phosphonate and sulfonate groups. In addition, bifunctional fibers gave much more excellent kinetic performances in column-mode uptake of Cu(II) than the monofunctional phosphonate fibers and resin.     

Utilization of a Biodegradable Mulch Sheet Produced from Poly(Lactic Acid)/Ecoflex?/Modified Starch in Mandarin Orange Groves

We have developed a mulch sheet made by inflation molding of PLA, Ecoflex^® and modified starch, which all have different biodegradabilities. A field test of use as an agricultural mulch sheet for mandarin oranges was carried out over two years. The mechanical properties of the mulch sheet were weakened with time during the field test, but the quality of the mandarin oranges increased, a result of the controlled degradation of the sheet. The most degradable modified starch degraded first, allowing control of the moisture on the soil. Accelerator mass spectroscopy was used for evaluation of the biomass carbon ratio. The biomass carbon ratio decreased by degradation of the biobased materials, PLA and modified starch in the mulch sheet.     

Anaerobic Biodegradation Tests of Poly(lactic acid) under Mesophilic and Thermophilic Conditions Using a New Evaluation System for Methane Fermentation in Anaerobic Sludge

Anaerobic biodegradation tests of poly(lactic acid) (PLA) powder were done at the thermophilic (55 °C) and mesophilic temperature (35 °C) under aquatic conditions [total solid concentrations of the used sludge were 2.07% (at 55 °C) and 2.24% (at 35 °C)] using a newly developed evaluation system. With this system, the evolved biogas is collected in a gas sampling bag at atmospheric pressure. This method is more convenient than using a pressure transducer or inverted graduated cylinder submerged in water. PLA was degraded about 60% in 30 days, about 80% in 40 days and about 90% in 60 days at 55 °C. On the other hand, the PLA degradation started in 55 days at 35 °C and degradation rate was much slower than at 55 °C.     

Gas phase oxidation of benzene to phenol using Pd-Cu composite catalysts. Effect of temperature,feeding gas and catalyst composition

Catalytic oxidation of benzene in the gas phase has been studied as a function of the catalyst composition, reaction temperature and the feed conditions of reactant gases, hydrogen, oxygen, benzene as well as diluting inert gas. The catalyst tested is composed of Pd and Cu(I) ions, both of which are supported on silica gel. If one of the two metal species is lacked from the catalyst, no catalytic activity appears. The product is almost exclusively phenol and some accompanying benzoquinone, in particular at lower temperatures, as minor byproduct.On leave from Hua-Dong Institute of Technology, Nanjing, People's Republic of China.