Prediction of output response probability of sound environment system using simplified model with stochastic regression and fuzzy inference

The traditional standard stochastic system models, such as the autoregressive (AR), moving average (MA) and autoregressive moving average (ARMA) models, usually assume the Gaussian property for the fluctuation distribution, and the well-known least squares method is applied on the basis of only the linear correlation data. In the actual sound environment system, the stochastic process exhibits various non-Gaussian distributions, and there exist potentially various nonlinear correlations in addition to the linear correlation between input and output time series. Consequently, the system input and output relationship in the actual phenomenon cannot be represented by a simple model. In this study, a prediction method of output response probability for sound environment systems is derived by introducing a correction method based on the stochastic regression and fuzzy inference for simplified standard system models. The proposed method is applied to the actual data in a sound environment system, and the practical usefulness is verified.     

Estimation of the value of ΔR/R for121Sb nucleus by means of Mössbauer spectroscopy and molecular orbital calculation

The¹²¹Sb Mössbauer spectra of rapidly frozen solutions of antimony compounds were observed. The isomer shifts were compared with the electron density at the antimony nucleus calculated with the ab initio molecular orbital method. A value ΔR/R=?(11±2)×10^?4 was derived for the 37.15 keV M1 transition of¹²¹Sb.     

Carbon dioxide fixation by microalgal photosynthesis using actual flue gas from a power plant

Applied Biochemistry and Biotechnology - CO2 fixation by microalgal cultures, a potential method for CO2 emissions mitigation, was studied in small (approx 2 m2) ponds using actual flue gas from...     

Improvement of substrate conversion to molecular hydrogen by three-stage cultivation of a photosynthetic bacterium,Rhodovulum sulfidophilum

In photosynthetic bacteria, after transition to light-anaerobic and nitrogen-deficient conditions, hydrogen evolution starts with expression of nitrogenase activity. Until the expression of enough activity,Rhodovulum sulfidophilum consumed substrates and converted them to poly(3-hydrox-ybutyrate) (PHB), resulting in a decrease in the proportion of substrate converted into hydrogen gas. To prevent conversion to PHB during the period when nitrogenase activity is derepressed, the authors employed a cultivation method consisting of three stages: cell growth, nitrogenase derepression, and hydrogen production. Cells cultivated by this method exhibited no lag time before the commencement of hydrogen evolution and gave an improved yield of hydrogen from the algal fermentative products.     

Two new steroidal derivatives from the fruit body of Chlorophyllum molybdites

Two new steroid derivatives, (22E,24R)-3alpha-ureido-ergosta-4,6,8(14),22-tetraene (1) and (22E,24R)-5alpha,8alpha-epidioxyergosta-6,9,22-triene-3beta-ol 3-O-beta-D-glucopyranoside (2) were isolated from the fruit bodies of Chlorophyllum molybdites (Agaricaceae). The structures were established by spectroscopic and chemical methods. These compounds exhibited cytotoxicity against Kato III cells.     

New method for standardization of electropherograms obtained in capillary zone electrophoresis

A new method for standardization of electropherograms obtained by capillary zone electrophoresis was proposed, where the migration time axis was replaced by the effective mobility axis. The mobility increase due to temperature increase by Joule heating and the relaxation effect of the potential gradient were eliminated successfully by introducing a temperature coefficient for mobility expression and a delay time, respectively. The precision of the mobility evaluated by the proposed conversion methods was evaluated for a model sample. By using the conversion method, almost the same electropherograms could be obtained even from the electropherograms originally obtained by using different hardware conditions.     

An ab initio MO study on structures and energetics of CH2Si2, CH2Si2, and CH2Si2

The geometric structures and isomeric stabilities of various stationary points in CH₂Si₂ neutral, cation and anion are investigated at the coupled-cluster singles, doubles (triples) (CCSD(T)) level of theory. For the geometrical survey, the basis sets used are of the cc-pVTZ for the neutral and cation. The final energies are calculated by the use of the CCSD(T) level of theory with the aug-cc-pVTZ basis set at their optimized geometries. To the competitive two-anion isomers, the aug-cc-pVTZ basis sets are applied. The global minimum (N-1) of the CH₂Si₂ neutral has a quite different framework from those of the C₃H₂ (cyclopropenylidene) and Si₃H₂ (trisilacyclopropenylidene) neutrals. No competitive low-lying isomers are found in the CH₂Si₂ neutral. The attractive conformer (C-1) is predicted for the most stable cation, where its framework is quite different from that of the neutral N-1. Both H atoms are connected to the same C atom, but each C–H bond length is different from each other. Two competitive anion isomers with positive (real) electron affinities are predicted. The framework of the most stable anion A-1 is quite similar to that of the cation C-1, whereas both H atoms are equally connected to the same C atom. The framework of the anion isomer A-2 is the same as that in the neutral N-1. The vertical and adiabatic ionization potentials from the most stable neutral N-1 are 9.02 and 8.71 eV, respectively. The adiabatic electron affinity of the lowest lying isomer N-1 is only 0.43 eV and the vertical electron detachment energy form the global minimum anion (A-1) is 2.02 eV. The multi-centered Si–H–Si bonds are found in the neutral, cation, and anion.     

Standardization of capillary zone electropherograms obtained by using field enhanced sample stacking

Migration times in a capillary zone electropherogram obtained by using the field enhanced sample stacking technique are strongly affected by the injected sample volume. That is, the migration times significantly decrease with the increase of the sample volume. To avoid inaccurate qualitative analysis due to the above phenomena, the time axis of the electropherograms was converted into an effective mobility axis using our conversion method taking account of the temperature increase in the separation tube and relaxation of the potential gradient of the separation field. After the conversion, accurate qualitative analysis was possible in spite of drastic change of the migration time, suggesting our conversion method could be successfully used for the standardization of electropherograms obtained even by using the stacking effect. The cause of the decrease of the migration time in the stacking process was briefly discussed.     

Theoretical study on isomeric stabilities of C2H2Si and its ionization potentials and electron affinities

The geometric structures and isomeric stabilities of various stationary points in C(2)H(2)Si neutral and its cation and anion are investigated at the coupled-cluster singles, doubles (triples) [CCSD(T)] level of theory. For the geometrical survey, the basis sets used are of the Dunning's correlation consistent basis sets of triple-zeta quality (cc-pVTZ) for the neutral and cation. For the anions, the cc-pVTZ basis sets with diffuse functions (aug-cc-pVTZ) are used. The final energies are calculated by the use of the CCSD(T) level of theory with the aug-cc-pVTZ basis set at their optimized geometries. To lower lying neutrals and cations, the Dunning's correlation consistent basis sets of quadruple-zeta quality (cc-pVQZ) are also applied. Both the global minima of the C(2)H(2)Si neutral and cation, N-1 (C(2v):(1)A(1)) and C-1 (C(2v):(2)B(2)), respectively, are silacyclopropenylidene conformers, having a CCSi ring with a C[Double Bond]C double bond. No competitive stable isomers exist in the present C(2)H(2)Si neutral. In the cation, however, the second lowest lying isomer C-2 lies 10.8 kJ/mol above the most stable C-1. The vertical and adiabatic ionization potentials from the lowest lying neutral N-1 are 9.83 and 8.97 eV, respectively, at the CCSD(T)/cc-pVQZ level of theory. The electron addition to the N-1 does not result in the anion with positive (real) electron affinities. On the other hand, the electron addition to the N-2 isomer produces the global minimum anion A-1 (C(2v):(2)B(1)) with the positive electron affinities of 1.13 eV. The second lowest lying anion isomer A-2 with silylenylacetylene conformer, produced from an electron addition to the N-3 neutral, very well competes with the A-1 after the zero-point vibrational energy corrections. The energy difference between the two lowest lying isomers of the neutral and its anion, N-1 and A-1, is only 0.39 eV.