Transfer of high-mannose-type oligosaccharides to disaccharides by endo-beta-N-acetylglucosaminidase from Arthrobacter protophormiae

Endo-beta-N-acetylglucosaminidase from Arthrobacter protophormiae (Endo-A) has transglycosylation activity, and high-mannose-type oligosaccharides are transferred to suitable glycosides as acceptor substrates. The acceptor specificity of Endo-A-catalyzed transglycosylation toward various disaccharides was investigated. To identify an effective acceptor for the transglycosylation by Endo-A, the reaction was carried out using various disaccharides. Endo-A transferred high-mannose-type oligosaccharides more efficiently to beta-linked disaccharides (cellobiose, gentiobiose, sophorose, and laminaribiose) than to alpha-linked disaccharides (isomaltose, maltose, nigerose, kojibiose, and trehalose) as acceptor substrates. The transglycosylation products, (Man)6GlcNAc-Glc-beta-Glc, were more rapidly hydrolyzed than (Man)6GlcNAc-Glc-alpha-Glc. These results indicate that Endo-A recognizes the anomeric configuration of the acceptor substrates, and beta-linked glycosides are suitable for the synthesis of transglycosylation products.     

Decreasing the initial irreversible capacity loss of graphite negative electrode by alkali-addition

The effect of alkali function group contained in electrode binder was investigated. Carboxy methyl cellulose (CMC) improved the initial irreversible capacity loss in graphite negative electrode. Lithium acetate also improved the initial cycle efficiency. On the other hand, ethyl cellulose (EC) and hydroxyl propyl methyl cellulose (HPMC), which do not have a carboxylic group, did not decrease the reductive electrolyte decomposition. After charge and discharge cycle, the surface film composition on the electrode with CMC was less than on the electrode without CMC. This suggests that a carboxylic group in the binder acted as a catalyst and promoted the solid electrolyte interphase (SEI) formation which prevents the excess electrolyte decomposition on the graphite electrode.     

Numerical Analysis of the Boundary Scattering Effect on Transport Properties in Bi-Sb Nanowires

In this study, we have numerically analyzed the transport properties of Bi-Sb nanowires, taking into account wire boundary scattering. Wire boundary scattering slightly decreased the Seebeck coefficient of Bi-Sb nanowires. This effect is due to the observation that boundary scattering and the mobility ratio of L-point electrons to T-point holes in the nanowires are smaller than those in bulk Bi-Sb because the wire boundary scattering suppresses the mobilities of L-point electrons and heavy holes. The largest Seebeck coefficient for all wire diameters was obtained when the Sb concentration was 5 at.%. The effective mass approached zero near 5 at.% Sb, and the small effective mass led to a large subband shift in each band. Thus, a small effective mass enhances the quantum effect at a fixed wire diameter, even if wire boundary scattering is taken into account.     

Upgrading and dewatering of raw tropical peat by hydrothermal treatment

In this study, hydrothermal upgrading and dewatering of raw tropical peat derived from Pontianak, West Kalimantan-Indonesia was evaluated at temperatures ranging from 150 to 380 °C, a maximum final pressure of 25.1 MPa and a residence time of 30 min. The moisture content of the raw peat was approximately 90 wt.%. Raw peat was hydrothermally upgraded without the addition of water in the laboratory scale. The yield of the solid products was between 53.0 and 99.7 wt.% and the effective calorific value of hydrothermally dewatered peat was between 17,290 and 29,209 kJ/kg following hydrothermal upgrading. In addition, the oxygen content in the solid product was varied from 38.4 to 15.6 wt.% after upgrading, while the carbon content from 55.2 to 77.8 wt.%. The hydrothermally upgraded peat fuel product also had an equilibrium moisture content of 2.3 wt.% and a maximum equilibrium moisture content of 17.6 wt.%. Upgraded peat is characteristically resistant to moisture adsorption at high humidity, which makes it promising for fuel based combustion. The change in the carbon-functional groups and their properties, as determined by FTIR and ¹³C NMR, are discussed in terms of the hydrothermal upgrading and dewatering process.     

Restoration of solid oxide fuel cell stacks after failure of partial cells

We investigated a solid oxide fuel cell stack that employs anode-supported planar cells in which two intermediate plates are installed every 10 cells to determine the influence of the separation and reconnection of the intermediate plates after high temperature operation. We showed that this separation and reconnection caused no significant degradation in stack performance. A 30-cell stack, which was constructed by removing two 10-cell sub-stacks from a 50-cell stack that had operated stably 1200 h, functioned well. The difference between the average voltages of the cells in the 50- and 30-cell stacks was less than 3% when the current density, fuel utilization, and oxygen utilization were 0.30 A cm⁻², 60%, and 15%, respectively. The 30-cell stack operated stably for about 1200 h with almost no degradation. These findings indicate that our stack can be restored after cells in the stack have broken down simply by removing the 10-cell sub-stacks that contain the broken cells and replacing them with undamaged 10-cell sub-stacks.     

X-ray photoemission spectroscopy of nitrogen-doped UNCD/a-C:H films prepared by pulsed laser deposition

Nitrogen-doped ultrananocrystalline diamond (UNCD)/hydrogenated amorphous carbon (a-C:H) films were deposited by pulsed laser deposition (PLD). Nitrogen contents in the films were controlled by varying a ratio in the inflow amount between nitrogen and hydrogen gases. The film doped with a nitrogen content of 7.9 at.% possessed n-type conduction with an electrical conductivity of 18 Ω^? 1 cm^? 1 at 300 K. X-ray photoemission spectra, which were measured using synchrotron radiation, were decomposed into four component spectra due to sp², sp³ hybridized carbons, C=N and C–N. A full-width at half-maximum of the sp³ peak was 0.91 eV. This small value is specific to UNCD/a-C:H films. The sp²/(sp³ + sp²) value was enhanced from 32 to 40% with an increase in the nitrogen content from 0 to 7.9 at.%. This increment probably originates from the nitrogen incorporation into an a-C:H matrix and grain boundaries of UNCD crystallites. Since an electrical conductivity of a-C:H does not dramatically enhance for this doping amount according to previous reports, we believe that the electrical conductivity enhancement is predominantly due to the nitrogen incorporation into grain boundaries.