Comparison of activities in selective catalytic reduction of NOx by C3H8 over Co/MFI, Fe/MFI, and H/MFI zeolite catalysts

The Co/MFI(SiO₂/Al₂O₃ = 30) were prepared by a precipitation method with NaOCl in alkali solutions exhibited high activities to N₂ at 250 °C for the selective catalytic reduction (SCR) of NO_x. These catalysts showed two UV–vis bands at 700 and 400 nm, indicating the presence of octahedral Co(III) as well as tetrahedral Co(II). The high SCR activity over such Co(III, II)/MFI(30) seems to come from Co(III)---O moieties. The Co(II)MFI(30) catalysts prepared from Co(II)Cl₂ exhibited low SCR activities due to the presence of tetrahedral Co(II) ions in MFI. Less CO formation occurred over Co/MFI catalysts. The Fe/MFI(30) catalyst exhibited high activity due to the presence of some Fe---O species in MFI but more amount of CO were produced during SCR. H/MFI(30) catalyst exhibited a good SCR activity. However, more amount of carbonaceous deposits were produced on it. The correlation between acid concentration and SCR activity was discussed over H/MFIs.     

Fully methylated oriC with negative superhelicity forms an oriC-membrane complex before initiation of chromosome replication

In an in vitro assay, the oriC DNA has been shown to bind to the outer membrane fraction only when it is hemimethylated (G.B. Ogden et al., Cell, 54, 127-135,1988). In this report, however, we demonstrated that a significant amount of the oriC DNA was recovered from the cells just before initiation with the oriC DNA being fully methylated. Formation of this preinitiation oriC-membrane complex and following initiation of chromosome replication were strongly inhibited by novobiocin, a DNA gyrase B subunit inhibitor, which reduced the superhelicity of the reporter plasmid in the cells. On the other hand, both reactions proceeded in the presence of nalidixic acid, a DNA gyrase A subunit inhibitor, which did not have the effect of reducing the superhelicity. These results suggest that the negative superhelicity of the DNA is required for preinitiation oriC-membrane complex formation and following initiation event of replication.     

Neutronic and thermodynamic feasibility of UF6-NpF6 fueled transmutation reactor

Transmutation of neptunium, which is contained in radioactive wastes discharged from nuclear reactors, was investigated as a substitutional method for geologic disposal. We proposed a transmutation reactor fueled with a mixture of gaseous ²³³UF₆ and ²³⁷NpF₆. Neutronic and thermodynamic analysis of the reactor revealed the feasibility of the concept. The reactor has two principal advantages: (1) use of the fuel gas enables on-line reprocessing, (2) ²³⁷Np can be transmuted by a high neutron flux. Our calculation indicated that the transmutation rate of ²³⁷Np was 335 g/year/MW_th, which is much larger than the annual yield of ²³²Np in PWR (6.19 g/year/MW_th).     

State feedback control of current-type PWM AC-to-DC converters

A control method for current-type PWM AC-to-DC converters that realizes a sinusoidal AC input current and unity power factor is discussed in detail. In such converters, an LC filter placed on the AC side may cause a resonant problem, especially in the transient condition. To overcome this problem, state feedback control is introduced, and a control strategy suitable for DC-output current control as well as AC-side current control is proposed. Circuit parameters and feedback coefficients in the AC-side current control system are optimized on the basis of an analysis in which the system is treated as a sampled-data system. A method of investigating parameters in the DC-side current control system is shown. To confirm the effectiveness of the control strategy and the validity of the analytical results, an experimental investigation of the basic characteristics of the system is made. As an example, this system is applied to controlling the current waveform in the reactor. The experimental results for this application are also included     

IAEA activities on Mmall and Medium Reactors: Harmonization of energy demand and supply in developing countries

Small and Medium Reactors (SMRs) are attractive in developing countries because of their unique features such as: better suitability for smaller electric grids, lower investment cost, smaller components and equipment to facilitate modularization, etc. Furthermore, other factors induced by SMR implementation, such as technical transfer promotion, domestic infrastructure improvement, stabilization of energy cost, and environmental protection put SMRs into a more favorable position. From the nuclear plant suppliers, many SMR designs are available for a wide range of applications. A questionnaire study, which the IAEA conducted in 1996, confirmed that several countries are interested in SMRs and that some SMRs are already in the detailed design stage. A projection shows that the total nuclear capacity would increase in all regions that consist mainly of developing countries in the near future. For a timely and broad implementation of SMRs, information exchange and cooperation are indispensable between nuclear suppliers and buyers. The IAEA continues to play a role in encouraging and assisting development and practical application of SMRs for harmonization of energy demand and supply in developing countries.     

Phase Formation and Microstructure of Titanium Oxides and Composites Produced by Thermal Plasma Oxidation of Titanium Carbide

The phase formation and microstructure of titanium oxides and composites produced by Ar–O₂ thermal plasma oxidation of titanium carbide powders were investigated in detail by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Relationships between the phase compositions and microstructures of the oxides were established by combined structural and phase analyses, in correlation with synthesis conditions and phase formation mechanisms. It is revealed that vapor condensation favored the formation of anatase, which existed as smaller particles, while liquid/solid oxidation favored the formation of rutile, which appeared as larger particles or composites. A higher oxygen input in the plasma gases (Ar + O₂) enhanced the formation of anatase due to impeded oxidation and evaporation. A small amount of Ti₄O₇ and Ti₃O₅ was detected in the larger particles coexisting with rutile or TiC. These suboxides were formed as intermediates in solid oxidation of TiC or precipitated from the Ti–C–O melt during cooling. Furthermore, extensive cracks, dislocations and stresses were observed in the monolithic rutile and composites, in association with the rapid quenching in this high-temperature in-flight oxidation process.     

The influence of carboxylate ions on the growth of β-FeOOH particles

Colloidal -FeOOH particles were produced by hydrolysis of FeCl₃ solutions doped with varied amounts of formate, lactate, oxalate, tartarate, pyromellitate and EDTA ions at 100 °C. The resulting particles were characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric-differential thermal analysis, Fourier transform-infrared spectroscopy, elemental analysis, and the adsorption of nitrogen and water. With increasing concentration of added carboxylate ions, the mean modal size of the particles formed increased at low concentrations and decreased after passing the maximum. The crystallite sizes also revealed a maximum on adding EDTA, oxalate and lactate ions, while they monotonically decreased with the addition of other ions. Doping with tartarate and pyromellitate ions by more than 7 and 10 mol%, respectively, produced amorphous particles containing a large amount of these ions. The particles formed with 20 mol% tartarate ions adsorbed water selectively.     

Decomposition Characteristics of an Artificial Biogas in a Low‐Pressure DC Glow Discharge

The decomposition characteristics of an artificial biogas, which is a mixture of CH ₄, CO ₂, and H ₂ S, using a low‐pressure DC glow discharge have been investigated. It is found that H ₂, CO, C ₂ H ₂, H ₂ O, CS ₂, and COS are produced from the artificial biogas in the glow discharge. About 65% of the hydrogen atoms in CH ₄ are converted into H ₂ at an input energy of 800 J, at which CH ₄ is completely decomposed, and the decomposition characteristics of the artificial biogas are minimally dependent on the H ₂ S additive. Further, H ₂ S has a tendency to be decomposed earlier than the other components of the artificial biogas. When the glow discharge is generated in the artificial biogas with H ₂ S, some of the carbon atoms are found to deposit on the electrodes and the wall of the discharge chamber. © 2013 Wiley Periodicals, Inc. Electr Eng Jpn, 186(1): 26–33, 2014; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.22304     

NMR-Guided Repositioning of Non-Steroidal Anti-Inflammatory Drugs into Tight Junction Modulators

Bioavailability is a major bottleneck in the clinical application of medium molecular weight therapeutics, including protein and peptide drugs. Paracellular transport of these molecules is hampered by intercellular tight junction (TJ) complexes. Therefore, safe chemical regulators for TJ loosening are desired. Here, we showed a potential application of select non-steroidal anti-inflammatory drugs (NSAIDs) as TJ modulators. Based on our previous observation that diclofenac and flufenamic acid directly bound various PDZ domains with a broad specificity, we applied solution nuclear magnetic resonance techniques to examine the interaction of other NSAIDs and the first PDZ domain (PDZ1) of zonula occludens (ZO)-1, ZO-1(PDZ1). Inhibition of ZO-1(PDZ1) is expected to provide loosening of the epithelial barrier function because the domain plays a crucial role in maintaining TJ integrity. Accordingly, diclofenac and indomethacin were found to decrease the subcellular localization of claudin (CLD)-2 but not occludin and ZO-1 at the apicolateral intercellular compartment of Madin–Darby canine kidney (MDCK) II cells. These NSAIDs exhibited 125–155% improved paracellular efflux of fluorescein isothiocyanate insulin for the Caco-2 cell monolayer. We propose that these NSAIDs can be repurposed as drug absorption enhancers for peptide drugs.     

Ligand-Installed Nanocarriers toward Precision Therapy

Development of drug-delivery systems that selectively target neoplastic cells has been a major goal of nanomedicine. One major strategy for achieving this milestone is to install ligands on the surface of nanocarriers to enhance delivery to target tissues, as well as to enhance internalization of nanocarriers by target cells, which improves accuracy, efficacy, and ultimately enhances patient outcomes. Herein, recent advances regarding the development of ligand-installed nanocarriers are introduced and the effect of their design on biological performance is discussed. Besides academic achievements, progress on ligand-installed nanocarriers in clinical trials is presented, along with the challenges faced by these formulations. Lastly, the future perspectives of ligand-installed nanocarriers are discussed, with particular emphasis on their potential for emerging precision therapies.