Corrosion evaluation of Au-Cu-Pd ternary alloys

The corrosion resistivity of single-phase Au-Cu-11 at% Pd alloys was evaluated by using a parameterQ which represented the total amount of anodic reaction in a potentiostatic polarization test. The result was compared with those for binary Au-Cu, ternary Au-Cu-11 at % Ag and some commercial alloys. The validity of usingQ as a corrosion parameter was confirmed by the good agreement between the analysed and calculated values of copper ion dissolved into the test solution. By replacing a part of the copper in Au-Cu alloys with palladium the corrosion resistivity can be greatly improved, but silver has no such significant effect. The value ofQ decreased by both treatments of homogenization and grain refinement of the alloy. One of the advantages of the alloy having a single-phase structure is that inhomogeneity in the distribution of the constituents is small even in the as-cast state, which results in a small galvanic effect.     

Oxidative coupling polymerization of racemic 3,3’-dihydroxy-2,2’-dimethoxy-1,1’-binaphthalene with copper(II)-(-)-sparteine complex

Summary The oxidative coupling polymerization of racemic 3,3’-dihydroxy-2,2’-dimethoxy-1,1’-binaphthalene with copper(II) chloride-(-)-sparteine [(-)Sp] in methanol at room temperature was carried out and the enantiomer-selectivity during the polymerization was examined. The (R)-monomer preferentially reacted, and the purity of the unreacted monomer reached 80%ee (S) after 15 h, while that of the polymerized monomer gradually decreased from 26%ee (R) as a function of the polymerization. The ratio of the rate constants of both enantiomers, s=k_R/k_S, was determined to be 2.3. The model coupling reaction of the mono-benzylated (R)-monomer with CuCl₂-(-)Sp showed that the R-configuration with respect to the carbon-carbon bonds between the monomer units was selectively constructed during the polymerization.     

Consequence analysis and safety verification of hydrogen fueling stations using CFD simulation

Now that environmental awareness is enhanced on a global basis, great hopes are placed on the expanded use of hydrogen stations and fuel-cell vehicles (FCVs) that economize hydrogen energy. Hydrogen stations must be safe and secure because they store large quantities of hydrogen under higher pressure than the hydrogen actually consumed by FCVs. Thus, multiple safety measures are taken to ensure that hydrogen does not leak from the stations. Furthermore, in the unlikely event of leakage, the damage needs to be kept on an allowable level. For this reason, it is necessary to understand the behavior of hydrogen gas leaking from the stations.     

Recognition and Excision Properties of 8‐Halogenated‐7‐Deaza‐2′‐Deoxyguanosine as 8‐Oxo‐2′‐Deoxyguanosine Analogues and Fpg and hOGG1 Inhibitors

Cellular DNA continuously suffers various types of damage, and unrepaired damage increases disease progression risk. 8‐Oxo‐2′‐deoxyguanine (8‐oxo‐dG) is excised by repair enzymes, and their analogues are of interest as inhibitors and as bioprobes for study of these enzymes. We have developed 8‐halogenated‐7‐deaza‐2′‐deoxyguanosine derivatives that resemble 8‐oxo‐dG in that they adopt the syn conformation. In this study, we investigated their effects on Fpg (formamidopyrimidine DNA glycosylase) and hOGG1 (human 8‐oxoguanine DNA N‐glycosylase 1). Relative to 8‐oxo‐dG, Cl‐ and Br‐deaza‐dG were good substrates for Fpg, whereas they were less efficient substrates for hOGG1. Kinetics and binding experiments indicated that, although hOGG1 effectively binds Cl‐ and Br‐deaza‐dG analogues with low K_m values, their lower k_cat values result in low glycosylase activities. The benefits of the high binding affinities and low reactivities of 8‐oxo‐dG analogues with hOGG1 have been successfully applied to the competitive inhibition of the excision of 8‐oxoguanine from duplex DNA by hOGG1.     

Synthesis of acetonitrile and related compounds from CO-H2-NH3 over Mo/SiO2

In the reaction of CO-H₂-NH₃ on Mo/SiO₂ catalysts, HCN is formed and is considered to be the principal intermediate for the formation of CH₃CN. At low temperature methylamine is also formed.     

Improved efficiency of Al0.36Ga0.64As solar cells with a ppnn structure

Improvement of efficiency of Al_0.36Ga_0.64As solar cells is advanced in two aspects of minority-carrier lifetime: reduction of majority-carrier concentration in the emitter and base layers, and reduction of deep levels in the back-surface-field (BSF) layer. A pp⁻n⁻n structure is proposed to optimize the use of the effect of reduced majority-carrier concentration, and its effectiveness verified in a preparatory experiment on Al_0.3Ga_0.7As solar cells. A very poor photoluminescence (PL) decay time (below 0.3 ns) of a BSF layer heavily doped with Si becomes 14-fold longer when Se is applied to the dopant instead of Si, resulting in an improvement of the external quantum efficiency near the absorption edge. These two aspects of this study lead to the realization of 16.6% efficiency under 1-sun, AM 1.5 global conditions with an Al_0.36Ga_0.64As solar cell.     

An improved prediction result of entropic‐FV model for vapor–liquid equilibria of solvent–polymer systems

In this work, entropic expressions of UNIFAC‐FV and Entropic‐FV models were evaluated by using an extensive database of infinite dilution vapor–liquid equilibrium (VLE) data of athermal systems containing polypropylene, polyethylene, and polyisobutylene. For the infinite dilution athermal systems, performance of the Entropic‐FV model was better than that of the UNIFAC‐FV model. Then, finite concentration VLE data of non‐athermal systems that consisted of 16 polymers and 36 solvents containing a large variety of solvent–polymer systems ranging from nonpolar to polar substances were considered to optimized 46 pairs of group interaction parameters of the Entropic‐FV model. For systems containing polar solvents of three types of solvents studied, revised group interaction parameters gave significant improvements from 17.9 to 13.0% average absolute deviation (AAD) of solvent activities. For overall results, improvements were achieved from 15.1 to 12.4% AAD. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1145–1153, 2005     

DNA taken into Bacillus subtilis competent cells by lysed-protoplast transformation is not ssDNA but dsDNA

Competent Bacillus subtilis incorporates whole-genome DNA (4215 kb) from the protoplast lysate of B. subtilis subtilis [Akamatsu, T. and Taguchi, H., Biosci. Biotechnol. Biochem., 65, 823-829 (2001)]. A continuous incorporated DNA is longer than 1500 kb [J. Biosci. Bioeng., 101, 257-262 (2006)]. Whether the incorporated DNA is single-stranded (ssDNA) or double-stranded DNA (dsDNA) has been studied by examining the transforming activity of the incorporated DNA. B. subtilis BEST7027 was used as the donor strain, which has a heterologous region consisting of the 145 kb region of the Synechocystis sp. PCC6803 genome and erm gene. The donor DNA was transferred to a wild-type or a recA recipient strain (AYG2 or SYN9), and protoplast lysate was prepared from the transformants and used as the donor DNA source for the second recipient strain (AU1 or AV1). The intergenote region showed a significant transforming activity. When DNase I was added to both cells collected from the first transformation mixture and the following protoplastization, the result was similar to that obtained without DNase I. All of the observations strongly suggest that the incorporated DNA is dsDNA, and the transformation of competent B. subtilis by DNA in protoplast lysate is different from that by purified DNA taken up conventionally.