Leaching test of gamma-emitting Cs,Ru, Zr,and U from neutron-irradiated UO2/ZrO2 solid solutions in non-filtered surface seawater

The leaching behaviors of gamma-ray radionuclides, Cs-137, Ru-103, and Zr-95, produced by neutron irradiation of UO₂/ZrO₂ solid solutions, in real surface seawater were investigated under atmospheric conditions. The fraction of radionuclide inventory leached in the seawater was in the order of Cs > Ru (～U) ? Zr, indicating that the fraction was significantly affected by the chemical state of the radionuclides. However, the amount of soluble nuclides was proportional to that of uranium regardless of whether the solid solutions were prepared under an oxidative or reductive environment. A tiny fraction of Ru was filtered out by a 3 kDa nominal molecular weight cut-off filter after the 160 d leaching test, suggesting a different behavior from its ionic form, but Cs and U did not form a colloid-like species in seawater.     

Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s)

Transition metal-catalyzed cross-coupling reactions of organic halides and pseudo-halides containing a C-X bond (X = I, Br, Cl, OTf, OTs, etc.) with organometallic reagents are among the most important transformations for carbon-carbon bond formation between a variety of sp, sp(2), and sp(3)-hybridized carbon atoms. In particular, researchers have widely employed Ni- and Pd-catalyzed cross-coupling to synthesize complex organic structures from readily available components. The catalytic cycle of this process comprises oxidative addition, transmetalation, and reductive elimination steps. In these reactions, various organometallic reagents could bear a variety of R groups (alkyl, vinyl, aryl, or allyl), but the coupling partner has been primarily limited to sp and sp(2) carbon compounds: alkynes, alkenes, and arenes. With alkyl coupling partners, these reactions typically run into two problems within the catalytic cycle. First, oxidative addition of alkyl halides to a metal catalyst is generally less efficient than that of aryl or alkenyl compounds. Second, the alkylmetal intermediates formed tend to undergo intramolecular beta-hydrogen elimination. In this Account, we describe our efforts to overcome these problems for Ni and Pd chemistry. We have developed new catalytic systems that do not involve M(0) species but proceed via an anionic complex as the key intermediate. For example, we developed a unique cross-coupling reaction of alkyl halides with organomagnesium or organozinc reagents catalyzed by using a 1,3-butadiene as the additive. This reaction follows a new catalytic pathway: the Ni or Pd catalyst reacts first with R-MgX to form an anionic complex, which then reacts with alkyl halides. Bis-dienes were also effective additives for the Ni-catalyzed cross-coupling reaction of organozinc reagents with alkyl halides. This catalytic system tolerates a wide variety of functional groups, including nitriles, ketones, amides, and esters. In addition, we have extended the utility of Cu-catalyzed cross-coupling reactions. With 1-phenylpropyne as an additive, Cu-catalyzed reactions of alkyl chlorides, fluorides, and mesylates with Grignard reagents proceed efficiently. These new catalytic reactions use pi-carbon ligands such as pi-allyl units or alkynes instead of heteroatom ligands such as phosphines or amines. Overall, these reactions provide new methodology for introducing alkyl moieties into organic molecules.     

Effect of Zn, Ni and Fe Impurities on Bi2Sr1.6La0.4CuO6+��

We measured the change of T _c with the doping of the magnetic and nonmagnetic impurity in Bi₂Sr_1.6La_0.4CuO_6+?? (Bi2201). The reduction of T _c is about 20% in samples with Zn (1.1%), Ni (1.0%), and Fe (1.2%), and a slight difference was observed among these samples. We also observed the resonance peak at the Zn-impurity site by scanning tunneling spectroscopy at 4.2 K. The observed resonance peak showed the four-fold symmetry, and appeared at approximately ?1.5 meV.     

Study of molecular behavior in oxidation of insulating oil using terahertz spectroscopy

The stock of aged power equipment is increasing and it is important to clarify the characteristics of deteriorated insulating oil. This paper describes a basic study of molecular behavior in the oxidation of insulating oil by terahertz spectroscopy. The oxidation of insulating oil was modeled by using various compositions of dodecane and 2‐octanol. The terahertz measurements indicated that signi?cant absorption related to hydroxyl groups (‐OH) occurred between 6 and 7 THz. The absorption band was also observed in accelerated aging alkylbenzene, which is used in power equipment as insulating oil and is sensitive to hydrogen bonds. © 2013 Wiley Periodicals, Inc. Electr Eng Jpn, 183(1): 9–15, 2013; Published online in Wiley Online Library (wileyonlinelibrary.com). DOI 10.1002/eej.22335     

Bubble and liquid flow characteristics during horizontal cold gas injection into a water bath

In refining processes such as the AOD process cold gas is blown horizontally into the molten metal bath of the processes. The spatial distribution of bubbles in the bath is one of the important factors influencing the efficiency of the processes. In this study, a water model study was carried out to understand the characteristics of bubbles and liquid flow generated by horizontal gas injection. The bubble and liquid flow characteristics were measured using an electro‐resistivity probe and a laser Doppler velocimeter, respectively. In the flow field near the nozzle the bubble characteristics for the horizontal cold gas injection can be predicted by empirical equations derived for isothermal gas injection systems. The liquid flow characteristics could not be measured in this region. On the other hand, in the region far from the nozzle the two characteristics for the cold gas injection became different from those for the isothermal gas injection because of enhanced buoyancy force acting on expanding cold bubbles due to heat transfer.     

Disinfection of Legionella pneumophila by ultrasonic treatment with TiO2

An ultrasonic treatment system, using a TiO₂ photocatalyst, was used to disinfect Legionella pneumophila. A kinetic study of the process indicates that TiO₂ significantly improves the disinfection process. The concentrations of viable cells were reduced to 6% of the initial concentrations in the presence of 0.2 g/ml TiO₂ after a 30 min of treatment period, while only an 18% reduction was observed in the absence of TiO₂. The potency of the disinfection could be enhanced, to some extent, by increasing the amount of TiO₂ used. Cell concentrations were decreased by an order of 3 within 30 min of treatment in the presence of 1.0 g/ml TiO₂. The disinfection power in the presence of TiO₂ versus Al₂O₃ was also compared and the findings showed that TiO₂ induced a higher cell killing. No significant effect of initial cell concentration on the disinfection was found in the range of 10²-10⁷ CFU/ml after a 30 min of treatment period. The mechanism of cell killing was investigated by examining the effects of OH radical scavengers such as ascorbic acid, histidine and glutathione. The disinfection power was reduced in samples that contained these radical scavengers, thus indicating the importance of OH radicals.     

Sulfated Hyaluronan Binds to Heparanase and Blocks Its Enzymatic and Cellular Actions in Carcinoma Cells

We examined whether sulfated hyaluronan exerts inhibitory effects on enzymatic and biological actions of heparanase, a sole endo-beta-glucuronidase implicated in cancer malignancy and inflammation. Degradation of heparan sulfate by human and mouse heparanase was inhibited by sulfated hyaluronan. In particular, high-sulfated hyaluronan modified with approximately 2.5 sulfate groups per disaccharide unit effectively inhibited the enzymatic activity at a lower concentration than heparin. Human and mouse heparanase bound to immobilized sulfated hyaluronan. Invasion of heparanase-positive colon-26 cells and 4T1 cells under 3D culture conditions was significantly suppressed in the presence of high-sulfated hyaluronan. Heparanase-induced release of CCL2 from colon-26 cells was suppressed in the presence of sulfated hyaluronan via blocking of cell surface binding and subsequent intracellular NF-κB-dependent signaling. The inhibitory effect of sulfated hyaluronan is likely due to competitive binding to the heparanase molecule, which antagonizes the heparanase-substrate interaction. Fragment molecular orbital calculation revealed a strong binding of sulfated hyaluronan tetrasaccharide to the heparanase molecule based on electrostatic interactions, particularly characterized by interactions of (−1)- and (−2)-positioned sulfated sugar residues with basic amino acid residues composing the heparin-binding domain-1 of heparanase. These results propose a relevance for sulfated hyaluronan in the blocking of heparanase-mediated enzymatic and cellular actions.     

Quantized Vortices and Diamagnetic Precursor to the Meissner State in High-T c Superconductors

We report the magnetic imaging for underdoped and optimally-dopedLa_2–x Sr _x CuO₄ (LSCO) thin films on single substrates and nearly optimallydoped YBa₂Cu₃O_7–x (YBCO) thin films on tricrystal substrates in the temperature range both below and above T _c using scanning SQUID microscopy. Below T _c, clear integer- and half-integer quantized vortices were observable. Above T _c, however, the inhomogeneous diamagnetic domains appeared. The local diamagnetic domains that led to the Meissner state were found in the broad temperature range for underdoped samples and in the narrow limited temperature range for optimally-doped samples. The results provide evidence that local diamagnetic domains are closely related to the pseudogap state. The continuous connection of the domain state above T _c with the state of a half-integer vortex at the tricritical point in the YBCO film below T _c also indicates that the diamagnetic domains are also closely related to the occurrence of d_x ^{2-y 2}-wave superconductivity.     

A 200 Mbit/s Synchronous TDM Loop Optical LAN Suitable for Multiservice Integration

This paper describes a 200 Mbit/s multiservice optical local area network (LAN) using a synchronous TDM loop structure. The LAN consists of a central supervisory node and multiple service nodes connected by an optical fiber loop. Each service node supports communication channels which have access to allocated time slots in TDM frames continuously circulating on the loop. Multiple independent communication paths of various speeds up to 140 Mbits/s and various modes including point-to-point, ring, and multicast, can be provided between the channels on the loop. The ring will be useful to support ring networks, such as a token ring. The structure of this LAN is quite suitable for integration of multiple services, including video, image, data, and voice, since each service can independently choose its own speed, access method, and mode. In this development, various LSI-based high-speed hardware technologies including compact E/O and O/E modules, GaAs 4 × 4 matrix switch LSI's, and high-speed TDM-processor LSI's, which are versatilely applicable to high-speed LAN's ranging from 100 Mbits/s up to 560 Mbits/s, have been successfully introduced and compact LAN equipment has been obtained. This paper deals mainly with the system and hardware structure of this LAN, together with high-speed hardware technologies. An outline of firmware and network operation, and an application example are also described.