Isotachophoretic analysis of surfactants

The qualitative and quantitative determination of anionic surfactants (sodium and lithium alkylsulfate, sodium dodecylbenzenesulfonate, sodium di-2-ethylhexyl sulfosuccinate, sodium and lithium perfluoroalkylcarboxylate, and lithium perfluorooctanesulfonate) were investigated by a capillary tube isotachophoresis using a potential gradient detector. The leading electrolyte solution was the mixture of acetonitrile and aqueous solution of histidine buffer containing calcium chloride. The terminating electrolyte solution was the aqueous solution of sodium octanoate. These electrolytes were effective for the analysis of the mixtures of strongly acidic surfactants.     

Sintering of the Mechanochemically Activated Powders of Hexagonal Boron Nitride

Pressureless sintering of hexagonal boron nitride (BN) was performed using a powder activated by mechano-chemical treatments. Physical properties of the sintered BN bodies depend on the type of starting powder and the conditions of the treatments. The BN body, which was obtained at 2000°C using an appropriate activated powder, was 99 wt% pure and was excellent in mechanical and physical properties, in spite of its low density (1.64 g/cm³).     

Effect of pressure on phase transition and morphology of bulk poly(trans-1,4-butadiene)

The effect of pressure on the melting, solid-solid transition, and crystallization of poly(trans-1,4-butadiene) (PTBD) was investigated using the pressure range of 1–3000 kg/cm². D.t.a. measurements showed that, the melting and transition temperatures increase with increasing pressure, whose pressure coefficients are 38°C per 1000 kg/cm² and 22°C per 1000 kg/cm², respectively. These values were in fairly close agreement with those calculated from the Clausius-Clapeyron equation. Morphological studies using electron microscope and small-angle X-ray scattering method revealed that, the samples crystallized with relatively small supercoolings under normal or high pressure, are formed of distinct lamellae 400–800 Å thick. The lamellar thickness was inappreciably dependent on crystallization pressure. The significant effect of pressure on crystallization was recognized in a tendency of the crystallinity to increase, with increasing crystallization pressure. This pressure effect was explained by the mechanism that, the increased pressure might make the packing of molecular chains in liquid, more dense and that the secondary crystallization might be accelerated, to increase the lateral dimensions of lamellae.     

Reuse of carwash water with a cellulose acetate ultrafiltration membrane aided by flocculation and activated carbon treatments

A reuse system for carwash water with a cellulose acetate (CA), hollow-fiber-type ultrafiltration membrane with the aid of flocculation and activated carbon treatments was proposed. The multi-blended flocculating agent containing bentonite, Al₂(SO₄)₃, sodium alginic acid and a cationic polyacrylamide showed higher removals of COD and turbidity for carwash wastewater compared with Al₂(SO₄)₃ or a water-soluble polymer individually. The effect of pure water permeability of the membrane on permeation flux in pretreated carwash wastewater by this agent was examined using three kinds of CA membranes whose molecular weight cut-offs were 150,000 Dalton. Permeation flux showed a higher value in the case of the membrane with higher pure water permeability. Practical scale experiments with a membrane area of 32 m² and 48 m² were conducted under a membrane pressure of 20 kPa. When carwash wastewater was pretreated with 50 mg/L of this multi-blended flocculating agent, permeation flux through the CA membrane with pure water permeability of 0.78 m³/(m²/h) at 100 kPa showed 1.0 m³/(m²/d) for more than 6 months. The COD, BOD and extract by n-hexane values of reuse water were 3.7-15.7 mg/L, 2.5-14.0 mg/L and below 0.5 mg/L, respectively.     

时效对Ti─51％Ni形状记忆合金组织和相变行为的影响

用示差扫描热分析仪（ＤＳＣ）和光学显微镜研究了时效对Ｔｉ－５１ａｔ％Ｎｉ形状记忆合金组织和相变行为的影响。加热冷却时，该合金发生了Ｂ_２　Ｒ　Ｍ转变。给出了Ｒ、Ｍ相变温度、热滞、相变热与时效温度、时效时间的关系。Ｒ相的形态类似于上贝氏体或魏氏组织。析出物的形态呈针状交叉分布。     

Topology optimization for fluid–thermal interaction problems under constant input power

This paper deals with density-based topology optimization considering fluid and thermal interactions, in which the Navier–Stokes and heat transport equations are coupled. We particularly focus on designing heat exchangers. In the engineering context, heat exchangers are designed while considering a certain amount of input power. Therefore it is important to maximize the performance of a heat exchanger under a constant input power. In this paper we propose a way to control the input power by introducing an extra integral equation. To be more precise, in the fluid analysis, the inlet pressure is determined by solving the extra integral equation together with the Navier–Stokes equation. By doing this we can keep the inlet power constant even when the flow channels are changed in the optimization process. Consequently, the system of equations of the fluid field takes an integrodifferential form. On the other hand, in the heat transport analysis, a single governing equation is defined for simultaneously modeling both the solid and fluid parts. The design variable is a fluid fraction whose distribution represents the topology of the solid and fluid domains. When designing heat exchangers, two different heat conditions are considered in the formulation of the optimization problems, namely temperature-dependent and temperature-independent heat sources. Through the numerical examples for designing flow channels in a heat exchanger, it is shown that distinct topologies can be obtained according to the input power and the heat source conditions.     

Link Prediction based on Structural Properties of Online Social Networks

Question-Answering Bulletin Boards (QABB), such as Yahoo! Answers and Windows Live QnA, are gaining popularity recently. Questions are submitted on QABB and let somebody in the internet answer them. Communications on QABB connect users, and the overall connections can be regarded as a social network. If the evolution of social networks can be predicted, it is quite useful for encouraging communications among users. Link prediction on QABB can be used for recommendation to potential answerers. Previous approaches for link prediction based on structural properties do not take weights of links into account. This paper describes an improved method for predicting links based on weighted proximity measures of social networks. The method is based on an assumption that proximities between nodes can be estimated better by using both graph proximity measures and the weights of existing links in a social network. In order to show the effectiveness of our method, the data of Yahoo! Chiebukuro (Japanese Yahoo! Answers) are used for our experiments. The results show that our method outperforms previous approaches, especially when target social networks are sufficiently dense.

Co-enzyme specificity of 3-isopropylmalate dehydrogenase from Thermits thermophilus HB8

The co–enzyme specificity of 3–isopropylmalate dehydrogenasefrom an extreme thermophile, Thermus thermophilus HB8, was changedfrom NAD to NADP by site–directed mutagenesis Based onsequence comparison of 3–isopropylmalate dehydrogenasesfrom various organisms with NAD– and NADP–dependentisocitrate dehydrogenases, Ser226, Ser253 and De279 of 3–isopropylmalatedehydrogenase were suggested as determining the co–enzymespecificity. These residues were replaced with the correspondingresidues of NADP–dependent isocitrate dehydrogenases;Arg, Gly and Tyr respectively. The single–mutated enzymes,S226R and I279Y, enhanced the activities towards NADP 10–and 3–fold respectively, whereas S253G reduced the activity.Among the multiple–mutated enzymes, the double–mutatedS226R/I279Y increased the catalytic efficiency against NADP( fold) and shifted the specificity for NAD towards NADP mostsignificantly ( 173–fold).     

Methanation of CO2 with the oxygen-deficient Ni(II)-ferrite under dynamic conditions

The continuous methanation of CO₂ has been accomplished over hydrogen-reduced Ni(II)-bearing ferrite (Ni_xFe_3–xO_4–; x=0.39, > 0) in a mixed gas flow of CO₂ and H₂ at 250–375 °C. The yield and the selectivity for the methanation were larger than 50% and 95%, respectively, at the initial stage of the process. They decreased to 31% and 89%, respectively, after 6 h methanation. The innovative results can be ascribed to the use of the new material; hydrogen-reduced Ni(II)-bearing ferrite. Its formation was evinced by chemical analyses and the increase in the lattice constant; the lattice constant of the Ni(II)-bearing ferrite (a₀ 0.8375 nm) was enlarged to 0.8379 nm by hydrogen reduction. The enlarged lattice constant was not changed during the methanation. These findings suggest that the methanation occurs at the oxygen-deficient site of the hydrogen-reduced Ni(II)-bearing ferrite, as well as the formation of water by combination of the incorporated oxygens with hydrogen. The methanation consists of three steps of the elementary reaction. First, the oxygen-deficient sites are formed by hydrogen reduction; second, CO₂ is reduced to elementary carbon and two oxygen ions which are incorporated into the oxygen-deficient sites; and third, the carbon deposited on the surface of the reduced ferrite is selectively hydrogenated to CH₄.