Precise metabolic flux analysis of coryneform bacteria by gas chromatography-mass spectrometry and verification by nuclear magnetic resonance

Precise metabolic flux analysis (MFA) by gas chromatography-mass spectrometry (GC-MS) and computer calculation was performed, and the consistency of the estimated results was verified by independently performed nuclear magnetic resonance (NMR) analysis. The precise estimation of flux by the integration method of the mass isotopomer signal, defined as the coefficient of variance (CV) of multiple determination, was investigated, and the results estimated using different data sets with the same magnitude of error were confirmed. The CV of multiple determinations was sufficiently small to discuss and compare the fluxes of a metabolic pathway. The estimated fluxes using the GC-MS data were cross-validated with the NMR data that were independently measured and not used for MFA. The developed method was successfully applied to the MFA of the growth phase of two different glutamate-producing coryneform bacteria, Corynebacterium glutamicum and C. efficiens. The difference in the growth rate between these two bacterial species was discussed while considering the results of MFA, including forward and backward (exchange) fluxes.     

A tolerance criterion for tar concentration in a model wood gas for a nickel/scandia-stabilized zirconia cermet anode in a solid oxide fuel cell

Durability of a nickel and scandia-stabilized zirconia cermet anode against toluene in hydrogen was evaluated in this paper. Anode deterioration was judged by the loss of elemental nickel from a surface of an anode. Elemental nickel loss was observed when the toluene concentration was 3 or 10 g/Nm³, steam to carbon ratio was 1, and current density was 0.5 A/cm² at both temperatures: 1073 K and 1173 K. Therefore the tolerance criterion must be less than 3 g/Nm³ in hydrogen in the experimental conditions. However, the deterioration can be mitigated to some extent by increasing the operating temperature, steam-to-carbon ratio, or current density. Anode deterioration was also mitigated when hydrogen concentration in the fuel gas was nearly identical to that of wood gas. The influence of hydrogen concentration in the fuel gas on deterioration may be substantial. The loss of elemental nickel could not be detected instantaneously by electrochemical diagnosis.     

Fabrication of Ni compound nanocrystal/nanocarbon composites by cooling of chloride-based fluxes

Unique Ni compound nanocrystals were successfully grown on carbon nanotubes (CNTs) by cooling a mixed chloride flux. Cup-stacked CNTs (CSCNTs) were used as the nanocarbon materials because of their structural features. The grown nanocrystals had a nanosheet structure, which was densely assembled and had a ribbon-like morphology. Therefore, the nanocrystal/CSCNT composites were expected to have a highly active surface area for the catalyst composites. The selected area electron diffraction pattern and the related radial intensity profiles indicated that the grown nanocrystals were Ni(OH)2. When the pristine CSCNTs were used as a starting material, the formation efficiency of the nanocrystal/CSCNT composites decreased because the pristine CSCNTs were not dispersed in the KCl-LiCl flux. Therefore, functionalization of the CSCNTs was carried out with VUV light irradiation. The dispersibility of the VUV light-treated CSCNTs increased in the KCl-LiCl flux in comparison with the pristine CSCNTs because oxygen-containing functional groups, such as -COOH and -CO, were introduced onto the surfaces of the CSCNTs.     

A Low‐Loss Medium‐Voltage Inverter Applying Series Connected General Purpose 1.2 kV Insulated Gate Bipolar Transistors with Accurate Voltage Balancing Techniques

This paper presents a medium‐voltage inverter applying series connected general‐purpose 1.2 kV insulated gate bipolar transistors (IGBTs) as a switching device to achieve low switching losses compared to inverters applying high‐voltage IGBTs with over 3 kV rating. Gate signal synchronization, which is essential to keep the balance of collector‐emitter voltages across the IGBTs, is achieved by magnetically coupling all gate lines using a simple two‐windings transformer. In order to obtain better voltage balancing, influence of stray capacitance distribution associated with an insulating substrate in a two‐in‐one IGBT module on the voltage sharing is investigated, and an optimized layout of heat sinks for the IGBT modules is proposed. To validate some performances concerning the device losses and the voltage sharing, a 170 kVA inverter based on three 1.2 kV IGBTs connected in series is built and evaluated. The experimental results are shown. Copyright © 2007 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Characteristics of tar,NOx precursors and their absorption performance with different scrubbing solvents during the pyrolysis of sewage sludge

Recently thermal utilizations of sewage sludge, especially pyrolysis and gasification, are regarded as promising technologies due to efficient utilization of fuel gas. In this study, characteristics of tar and NOx precursors were investigated during the pyrolysis of sewage sludge. Moreover, absorption performance for tar and NOx precursors were also studied by using four kinds of scrubbing mediums: cooking oil, diesel oil, BDF and water. The results showed that nitrogenous light PAHs were the major components of nitrogenous tar produced from the pyrolysis of sewage sludge. As for gravimetric tar and major nitrogenous tar compounds removal, cooking oil was the most suitable absorbent. With respect to NOx precursors, it was concluded that HCN, sharing of about 39.5% of total nitrogen of the sewage sludge, was the main NOx precursor gas whereas NH₃ content could be neglected. Absorption capacity of hydrophobic scrubbing mediums against NOx precursor gases could be arranged as followed: diesel oil > cooking oil > BDF.     

1100 kV气体绝缘双断口断路器的开发与产品化

开发了一种用于气体绝缘组合电器(GIS)的1100kV50kASF6气体双断口断路器(GCB)。研究了这种断路器的各种特性,并成功完成了在绝缘、开断和机械性能等方面的型式试验。实现了GCB的小型化和轻量化。这种新开发的GCB已应用在中国特高压交流示范工程的GIS中,并已于2009年年初投入使用。     

Crystallization process and some properties of novel transparent machinable calcium-mica glass-ceramics

Bulk glass having a calcium-mica composition (Ca_0.5Mg₃AlSi₃O₁₀F₂) is homogeneous glass. The crystallization mechanism of the mica is surface crystallization and transparency is lost completely when crystallization occurs on the surface. In this study, by decreasing SiO₂ and increasing CaO and Al₂O₃ from the chemical composition of Ca_0.5Mg₃AlSi₃O₁₀F₂, and moreover by replacing a small amount of K₂O instead of CaO, the phase separation appears in the glasses. Because of this phase separation, the mica begins to be crystallized not only on the surface but also in the bulk at lower temperatures. Consequently, the novel transparent machinable mica glass-ceramic can be obtained by heating the glasses having the chemical composition of Ca_0.6Mg₃Al_1.2Si_2.8O₁₀F₂ and K_0.01Ca_0.595Mg₃Al_1.2Si_2.8O₁₀F₂. As a larger amount of calcium-mica is separated, the bending strength decreases and the fracture toughness increases. Furthermore, by replacing K⁺ ion instead of Ca²⁺ ion in the interlayer of calcium-mica, the interlayer bonding strength becomes high, resulting in the increase of the bending strength.     

Influences of saturation ratios on crystallization of anatase titanium dioxide by a titanium alkoxide hydrolysis

Influences of supersaturation in a tetraethyl orthotitanate (TEOT) solution on the degree of crystallinity of product particles in the case of a hydrolysis reaction of TEOT were indicated and the crystallization phenomena of anatase titanium dioxide (TiO₂) were discussed. Changes in saturation ratios with experimental durations were examined for the various amount of acetylacetone added into a TEOT solution. At the initial stages of TEOT hydrolysis operations, the degree of crystallinity of product particles was lower for the longer hydrolysis durations but the degrees became almost constant in the later stages of TEOT hydrolysis operations, although the supersaturation of titanium oxide in a TEOT solution was remained. Rapid increase in supersaturation of titanium oxide in a TEOT solution and consequent nucleation of amorphous titanium oxide would be restrained by addition of acetylacetone into a TEOT solution because the concentrations of titanium oxide in a saturated TEOT solution increased with the amount of acetylacetone.     

Adsorption of cationic monomeric and gemini surfactants on montmorillonite and adsolubilization of vitamin E

Adsorption of a cationic gemini surfactant (1,2-bis(dodecyldimethylammonio) ethane dibromide, 12-2-12) and the corresponding monomeric surfactant (dodecyltrimethylammonium bromide, DTAB) on montmorillonite has been characterized with a combination of adsorption isotherm, interlayer spacing and FT-IR spectroscopic data. Adsolubilization of vitamin E into the adsorbed surfactant layers has also been studied. The adsorption isotherm data reveal that the adsorption of the two surfactants is driven by the two factors: one is the cation exchange that occurs on the interlayer basal planes and the other is the hydrophobic interaction between hydrocarbon chains of the surfactants. Although the adsorbed amount measured in the saturation region (in mol g(-1)) is almost identical for the two surfactants, the conformation of the intercalated surfactant molecules differs significantly from each other. The adsorption of DTAB results in a lateral bilayer arrangement in the limited interlayer space, whereas 12-2-12 gives a normal bilayer arrangement in the expanded interlayer space. Adsolubilization of vitamin E takes place into the adsorbed surfactant layers, and interestingly, all the vitamin E molecules added in the montmorillonite suspensions are hybridized at lower surfactant concentrations due to the great specific surface area of the clay material. Since the maximum adsolubilization amount is usually obtained just below the critical micelle concentration, the gemini surfactant is deemed to be more efficient than the corresponding monomeric one to achieve the great adsolubilization amount.     

Transient kinetic studies of pH-dependent hydrolyses by exo-type carboxypeptidase P on a 27-MHz quartz crystal microbalance

pH-Dependent kinetic parameters (k(on), k(off), and k(cat)) of protein (myoglobin) hydrolyses catalyzed by exo-enzyme (carboxypeptidase P, CPP) were obtained by using a protein-immobilized quartz crystal microbalance (QCM) in acidic aqueous solutions. The formation of the enzyme-substrate (ES) complex (k(on)), the decay of the ES complex (k(off)), and the formation of the product (k(cat)) could be analyzed by transient kinetics as mass changes on the QCM plate. The Kd (k(off)/k(on)) value was different from the Michaelis constant Km calculated from (k(off) + k(cat))/k(on) due to k(cat) > k(off). The rate-determining step was the binding step (k(on), and the catalytic rate k(cat) was faster than other k(on) and k(off) values. In the range of pH 2.5-5.0, values of k(on) gradually increased with decreasing pH showing a maximum at pH 3.7, values of k(off) were independent of pH, and k(cat) increased gradually with decreasing pH. As a result, the apparent rate constant (k(cat)/Km) showed a maximum at pH 3.7 and gradually increased with decreasing pH. The optimum pH at 3.7 of k(on) is explained by the optimum binding ability of CPP to the COOH terminus of the substrate with hydrogen bonds. The increase of k(cat) at the lower pH correlated with the decrease of alpha-helix contents of the myoglobin substrate on the QCM.