Nanopillar array chip integrated with on-line stacking for fast DNA separation with high sensitivity and high resolution

Recent developments of nanofabrication techniques have created a trend switching from randomly ordered polymeric matrices, such as gel, to highly ordered sieving nanostructures in the separation of biomolecules. These nanostructures have enormous potential for fast separation of biomolecules, while nanostructure-based separation techniques suffer from critical scaling problems; they are efficient in handling less than nanoliter amounts of sample fluids, but most biomolecule samples are available in a liquid volume that is over several microliter, leading to a reduction in sensitivity and resolution. In this study, we developed a nanopillar array chip integrated with an easy and rapid on-line stacking method and achieved fast DNA separation with high sensitivity and high resolution. The developed on-line stacking method is based on the balance of two forces driven by electric fields: electroosmotic flow (EOF) and electrophoresis. The EOF mobility from the microchannel to the nanopillar-channel is drastically decreased, while, on the other hand, electrophoresis has constant mobilities in the whole length of the channels. The on-line stacking was realized at the well-balanced position of the two forces, and the on-line stacking using the nanopillar array chip can also be achieved within 10 s by just applying electric voltages without any other special reagents and materials. After applying on-line stacking using the nanopillar array chip, the relative fluorescence intensity increased 1,000-fold, and the resolution was twice as good as that without on-line stacking.     

New monitoring approach for metabolic dynamics in microbial ecosystems using stable-isotope-labeling technologies

We have developed a new approach for monitoring the metabolic dynamics in microbial ecosystems using a combination of DNA fingerprinting and metabolome analysis based on stable-isotope-labeling technologies. Stable-isotope probing of DNA (DNA-SIP) has been used previously for the evaluation of cross-feeding in microbial communities. For the development and validation of our monitoring approach, fecal microbiota were analyzed with stable-isotope-labeled glucose used as the sole carbon source. In order to link the metabolic information and the microbial variability, we performed metabolic–microbial correlation analysis based on nuclear magnetic resonance (NMR) profiles and denaturing gradient gel electrophoresis (DGGE) fingerprints, which successfully identified the glucose-utilizing bacteria and their related extracellular metabolites. Moreover, our approach revealed information regarding the carbon flux, in that the “first” wave of extracellular metabolites secreted by the glucose-utilizing bacteria were incorporated into the “secondary” group of substrate-utilizing bacteria, and that this “secondary” group further produced their own secondary metabolized substrates. Thus, this approach is a powerful tool for monitoring the metabolic dynamics in microbial ecosystems and allows for the tracking of the carbon flux within a microbial community.     

Performance evaluation of membrane on catalyst module for hydrogen production from natural gas

We have been developing a hydrogen production module with a Pd-based membrane on catalyst (MOC) from natural gas. The MOC module is expected to be more compact and cheaper than the conventional hydrogen production module. To evaluate the hydrogen production performance of the MOC module and to clear the factor that dominates the effective hydrogen production, we compared the reforming performance of the catalytic support without hydrogen permeable membrane and the MOC module at various reaction conditions. As a result, it was cleared that hydrogen permeation through the membrane improves the methane conversion drastically in the MOC module by comparing with the support only module and changing the experimental conditions.     

Electrolyte properties of 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids for lithium secondary batteries

The physicochemical and electrochemical properties of three 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids with various alkyl chain lengths were investigated. The temperature dependences of density, viscosity, and ionic conductivity were obtained by precise measurements. Electrolyte properties of these room-temperature ionic liquids were also examined from the viewpoint of their uses in lithium secondary batteries ([LiCoO₂ positive electrode|electrolyte|lithium metal negative electrode]). It was found that the alkyl chain length affects the charge–discharge performances of cells.     

A study of electrical characteristic changes in MOSFET by electron beam irradiation

Mechanisms for electrical characteristic changes in MOSFET caused by electron beam irradiation were studied using a SEM-based nano-probing system. A shift in V_th occurs when a hole is trapped in a defect (oxygen vacancy) in the gate dielectric layer. Holes are generated when the plasmon is excited by electron beam irradiation. Further, an electric field is created by the positive charge-up resulting from electron beam irradiation of the ILD, causing an increase in leakage between gate and drain leading to an increase in I_off. This study shows that advanced devices can be measured using a SEM-based nano-probing system without inducing electrical characteristic changes by optimizing the measurement conditions such as acceleration voltage, electron beam current, image magnification, ILD thickness, and electron beam irradiation time.     

Characterization of the AIN–W Interface in a Cofired Multilayer AIN Substrate

The AIN–W Interfaces in a cofired multilayer AIN substrate were observed using an optical microscope, scanning electron microscope (SEM) and transmission electron microscope (TEM). Optical and SEM observations showed an intricate intricatelocking AIN-W grain structure at the interface. After the W pad was removed from the substrate with a NaOH etchant, the surface morphology of the W metal at the interface side was found to be very rough, with a small-grain microstructure compared with that at the free surface side. Electron microprobe analyses using SEM revealed that there was no diffusion of either W or Al at the interface at the order of a few micrometer's resolution. Bright-field images, dark-field images and selected area electron diffraction (SAD) patterns using TEM indicated there was no secondary phase between AIN and W. However, scanning transmission electron microscopy using an energy dispersive X-ray detector revealed that there was a 200-nm thick W diffusion layer from the interface into the AIN ceramics. It was concluded that the high adhesion strength between the W conductor and the AIN substrate (>20 MPa) was not due to any secondary phase but to mechanical interlocking of AIN and W during cofiring.     

Electrolytic reduction of U(VI) to U(IV) in acidic chloride and acidic sulfate solutions

In order to examine the applicability of the electrolytic reduction process of U(VI) (originally developed for the chloride system by PNC) to the sulfate solution system, a fundamental study was made. In this study, the concentrations of various chemical species in the catholytes were calculated at 298 K at various percentages of uranium reduction, taking the chloro-complex and sulfato-complex formation reactions of uranium into consideration. The polarization characteristics of the electrolytic reduction of uranyl chloride and uranyl sulfate were determined, using titanium and platinum cathodes, respectively, at 303 ± 1 K. In conjunction with this process, the electrical conductivity of the catholyte, the electrical resistivity of the cation exchange membrane, and the diffusion coefficient of uranyl sulfate were also determined.     

Photoluminescence of nitrogen-doped anatase

Photoluminescence depending on nitrogen concentration was investigated using anatase-type TiO₂ prepared by the calcination of a mixture of titanyl sulfate hydrate and urea. The substitutional ratio (x) of nitrogen in TiO₂ was successfully varied from 0.004 to 0.022 by changing the molar ratio of the mixture. The absorbance at 380–560 nm due to the formation of mid-gap states was proportional to the substitutional ratio of nitrogen controlled by the preparation conditions. In contrast, the fluorescent intensity at 382 nm originating from the band-to-band transition monotonically decreased with an increase in the substitutional ratio with an expansion of the anatase lattice. On the other hand, the maximum intensity of photoluminescence at 560 nm excited at 350 nm, which could be associated with the transition from the conduction band to the mid-gap states, was observed at x = 0.01. The optimal substitutional ratio for the emission was almost agreed with that for the photocatalytic decomposition of methylene blue and acetaldehyde under visible-light illumination. The photoluminescence was fundamentally determined by the balance between photoexcitation originating from a sufficient number of mid-gap states and deactivation of excited electrons and holes due to lattice distortion or defective states induced with the nitrogen doping.     

Examination of the dual‐band microwave wireless access system using radio on fiber technique

The Radio on Fiber (ROF) technique has great potential in wireless communication systems. In this paper, we report on a fundamental examination of microwave wireless access systems based on Radio on Fiber. First, we designed and constructed examination systems by applying dual band (2.4 and 5 GHz) multiservice transmission systems and confirmed that there was sufficient performance through a transmission experiment. Then, application of FP‐LD (Fabry Perot Laser Diode) was considered in order to reduce the system cost, and for the most part degradation of the transmission characteristics was not observed when FP‐LD was used. Finally, a BIDI (bidirectional) module which integrated LD and PD within one package was made to further reduce costs. By measuring the transmission performance, applying the BIDI module to ROF systems was shown to be effective. © 2007 Wiley Periodicals, Inc. Electr Eng Jpn, 160(4): 32–40, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20471     

N-Alkylation of chitin and some characteristics of the novel derivatives

Summary Introduction of simple alkyl groups at the C-2 nitrogen of chitin and some properties of the resulting N-alkyl-chitins have been examined. Chitosan was fully deacetylated and treated with three kinds of aldehydes, formaldehyde, acetaldehyde, and pentanal. The Schiff bases of chitosan, whose extents of substitution were dependent on the amount of aldehydes, were reduced with sodium cyanoborohydride to N-alkylated chitosans. The N-alkyl-chitosans were then transformed into the corresponding N-alkyl-chitins by acetylation with acetic anhydride followed by transesterification to remove partly formed O-acetyl groups. The resulting N-methyl-, ethyl-, and pentyl-chitins were amorphous and showed improved affinity for organic solvents. Received: 13 December 2001/Revised version: 11 January 2002/Accepted: 17 January 2002