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61.
62.
Ryoji Kobori Tomonori Ohba Takaomi Suzuki Taku Iiyama Sumio Ozeki Michio Inagaki Akihiro Nakamura Masato Kawai Hirofumi Kanoh Katsumi Kaneko 《Adsorption》2009,15(2):114-122
N2 adsorption isotherms of molecular sieve carbon were measured at 77 K and 303 K. The Ar adsorption isotherms of molecular
sieve carbon samples were also measured at 303 K. The grand canonical Monte Carlo (GCMC) simulation technique was applied
to calculate the N2 and Ar adsorption isotherms at 303 K using the ultramicropore volume determined by H2O adsorption. The comparative method of experimental and simulated isotherms of supercritical N2 and Ar at 303 K gave the width of the micropore mouth of the molecular sieve carbon, which can be applied to the ultramicropore
width determination for other noncrystalline porous solids. 相似文献
63.
Stefano Freguia Masaki Masuda Seiya Tsujimura Kenji Kano 《Bioelectrochemistry (Amsterdam, Netherlands)》2009,76(1-2):14
Lactococcus lactis is a gram-positive, normally homolactic fermenter that is known to produce several kinds of membrane associated quinones, which are able to mediate electron transfer to extracellular electron acceptors such as Fe3+, Cu2+ and hexacyanoferrate. Here we show that this bacterium is also capable of performing extracellular electron transfer to anodes by utilizing at least two soluble redox mediators, as suggested by the two-step catalytic current developed. One of these two mediators was herein suggested to be 2-amino-3-dicarboxy-1,4-naphthoquinone (ACNQ), via evaluation of standard redox potential, ability of the bacterium to exploit the quinone when exogenously provided, as well as by high performance liquid chromatography coupled with UV spectrum analysis. During electricity generation, L. lactis slightly deviated from its normal homolactic metabolism by excreting acetate and pyruvate in stoichiometric amounts with respect to the electrical current. In this metabolism, the anode takes on the role of electron sink for acetogenic fermentation. The finding that L. lactis self-catalyses anodic electron transfer by excretion of redox mediators is remarkable as the mechanisms of extracellular electron transfer by pure cultures of gram-positive bacteria had previously never been elucidated. 相似文献
64.
Consider the stationary Navier–Stokes equations in a bounded domain whose boundary consists of multi-connected components.
We investigate the solvability under the general flux condition which implies that the total sum of the flux of the given
data on each component of the boundary is equal to zero. Based on our Helmholtz–Weyl decomposition, we prove existence of
solutions if the harmonic part of the solenoidal extension of the given boundary data is sufficiently small in L
3 compared with the viscosity constant.
Dedicated to Professor Giovanni P. Galdi on the occasion of his 60th birthday. 相似文献
65.
Shoji T Higashi J Ito S Okujima T Yasunami M Morita N 《Organic & biomolecular chemistry》2012,10(12):2431-2438
Arylethynyl-2H-cyclohepta[b]furan-2-ones reacted with 7,7,8,8-tetracyanoquinodimethane (TCNQ) in a formal [2 + 2] cycloaddition reaction, followed by ring opening of the initially formed cyclobutene derivatives, to afford the corresponding dicyanoquinodimethane (DCNQ) chromophores in excellent yields. The intramolecular charge-transfer (ICT) interactions between the 2H-cyclohepta[b]furan-2-one ring and DCNQ acceptor moiety were investigated by UV/Vis spectroscopy and theoretical calculations. The redox behavior of the novel DCNQ derivatives was examined by cyclic voltammetry (CV) and differential pulse voltammetry (DPV), which revealed their multistep electrochemical reduction properties depended on the number of DCNQ units in the molecule. Moreover, a significant color change was observed by visible spectroscopy under electrochemical reduction conditions. 相似文献
66.
Taku Saiki 《Journal of Electrostatics》2012,70(4):400-406
A theory for generating an ultra-high voltage using a flame column (weakly ionized plasma) and a normal high-voltage (HV) power supply is presented. A high-voltage generator adapted based on this theory was fabricated, and experiments on high voltage generation were carried out. As a result, high voltages were observed between an electron cloud in front of the flame column and the positive electrode in the experiment, and highly positive charges were stored efficiently on the large positive electrode. The experimental results proved that the output voltage is three times higher than that of the output voltage of the HV power supply whenever the gas flow velocity is close to 0. A maximum output voltage was obtained for the output voltage of the HV power supply, which was 15 times higher than the output voltage of the HV power supply. The generated voltage and the output current for the output voltage of the HV power supply were investigated, and the temporal dependence of the charging current was also measured. The use of this method made it possible to obtain a high voltage and high electric field in a large space. Furthermore, the realistic possibility of achieving a 10-MV using this method was shown. 相似文献
67.
Pietro Asinari Taku Ohwada Eliodoro Chiavazzo Antonio F. Di Rienzo 《Journal of computational physics》2012,231(15):5109-5143
The artificial compressibility method (ACM) for the incompressible Navier–Stokes equations is (link-wise) reformulated (referred to as LW-ACM) by a finite set of discrete directions (links) on a regular Cartesian mesh, in analogy with the lattice Boltzmann method (LBM). The main advantage is the possibility of exploiting well established technologies originally developed for LBM and classical computational fluid dynamics, with special emphasis on finite differences (at least in the present paper), at the cost of minor changes. For instance, wall boundaries not aligned with the background Cartesian mesh can be taken into account by tracing the intersections of each link with the wall (analogously to LBM technology). LW-ACM requires no high-order moments beyond hydrodynamics (often referred to as ghost moments) and no kinetic expansion. Like finite difference schemes, only standard Taylor expansion is needed for analyzing consistency. Preliminary efforts towards optimal implementations have shown that LW-ACM is capable of similar computational speed as optimized (BGK-) LBM. In addition, the memory demand is significantly smaller than (BGK-) LBM. Importantly, with an efficient implementation, this algorithm may be among the few which are compute-bound and not memory-bound. Two- and three-dimensional benchmarks are investigated, and an extensive comparative study between the present approach and state of the art methods from the literature is carried out. Numerical evidences suggest that LW-ACM represents an excellent alternative in terms of simplicity, stability and accuracy. 相似文献
68.
Taku Katayama Kiyotaka Onitsuka Shigetoshi Takahashi 《Journal of organometallic chemistry》2000,610(1-2):31-37
Treatment of ruthenium complexes [CpRu(AN)3][PF6] (1a) (AN=acetonitrile) with iron complexes CpFe(CO)2X (2a–2c) (X=Cl, Br, I) and CpFe(CO)L′X (6a–6g) (L′=PMe3, PMe2Ph, PMePh2, PPh3, P(OPh)3; X=Cl, Br, I) in refluxing CH2Cl2 for 3 h results in a triple ligand transfer reaction from iron to ruthenium to give stable ruthenium complexes CpRu(CO)2X (3a–3c) (X=Cl, Br, I) and CpRu(CO)L′X (7a–7g) (L′=PMe3, PMe2Ph, PMePh2, PPh3, P(OPh)3; X=Br, I), respectively. Similar reaction of [CpRu(L)(AN)2][PF6] (1b: L=CO, 1c: P(OMe)3) causes double ligand transfer to yield complexes 3a–3c and 7a–7h. Halide on iron, CO on iron or ruthenium, and two acetonitrile ligands on ruthenium are essential for the present ligand transfer reaction. The dinuclear ruthenium complex 11a [CpRu(CO)(μ-I)]2 was isolated from the reaction of 1a with 6a at 0°C. Complex 11a slowly decomposes in CH2Cl2 at room temperature to give 3a, and transforms into 7a by the reaction with PMe3. 相似文献
69.
The zero‐viscosity limit for an initial boundary value problem of the linearized Navier‐Stokes equations of a compressible viscous fluid in the half‐plane is studied. By means of the asymptotic analysis with multiple scales, we first construct an approximate solution of the linearized problem of the Navier‐Stokes equations as the combination of inner and boundary expansions. Next, by carefully using the technique on energy methods, we show the pointwise estimates of the error term of the approximate solution, which readily yield the uniform stability result for the linearized Navier‐Stokes solution in the zero‐viscosity limit. © 1999 John Wiley & Sons, Inc. 相似文献
70.
Prof. Dr. Taku Shoji Sho Takagaki Yukino Ariga Akari Yamazaki Mutsumi Takeuchi Prof. Dr. Akira Ohta Dr. Ryuta Sekiguchi Dr. Shigeki Mori Prof. Dr. Tetsuo Okujima Prof. Dr. Shunji Ito 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(9):1931-1935
In this paper, we describe an efficient and atom-economical synthesis of highly functionalized pyrroles, pentafulvenes, and pyrrolopyridines by [2+2] cycloaddition–retroelectrocyclization of N-substituted propargylamines with tetracyanoethylene, followed by the treatment of the resulting tetracyanobutadiene derivatives with silica gel. In this reaction, silica gel plays an important role to promote the intramolecular cyclization to afford the heterocyclic products from the tetracyanobutadiene intermediates. The products were obtained selectively depending on the substituent on the nitrogen atom of the starting propargylamines. 相似文献