Inhibitory effect of high concentrations of ferric ions on the activity of Acidithiobacillus ferrooxidans

The influence of high concentrations of ferric ions on the biochemical activity of Acidithiobacillus ferrooxidans was studied using intact cells. The specific oxidation rate of ferrous ions decreased with increasing ferric ion concentration. Lineweaver-Burk plots revealed typical competitive inhibition kinetics, because the slopes varied with the ferric ion concentration. A linear relationship between the slope and the square of the ferric ion concentration revealed that the iron-oxidizing enzyme system of A. ferrooxidans was competitively inhibited by about two molecules of ferric ion. The kinetic equation based on this inhibition model agreed with the experimental observation at a high ferric ion concentration where the bacterium is usually exposed in bioleaching and biooxidation plants.     

Temperature-dependent near-infrared spectra of bovine serum albumin in aqueous solutions: spectral analysis by principal component analysis and evolving factor analysis

Fourier transform near-infrared (FT-NIR) spectra have been measured for bovine serum albumin (BSA) in an aqueous solution (pH 6.8) with a concentration of 5.0 wt% over a temperature range of 45-85 degrees C. Not only conventional spectral analysis methods, such as second-derivative spectra and difference spectra, but also chemometrics, such as principal component analysis (PCA) and evolving factor analysis (EFA), have been employed to analyze the temperature-dependent NIR spectra in the 7500-5500 and 4900-4200 cm-1 regions of the BSA aqueous solution. Intensity changes of bands in the 7200-6600 cm-1 and 4650-4500 cm-1 regions in the difference spectra indicate variations of the hydration and secondary structure of BSA in the aqueous solution, respectively. The plot of a band intensity at 7080 cm-1 in the different spectra shows a clear turning point at 63 degrees C, revealing that a significant change in the hydration occurs at about 63 degrees C. The forward and backward eigenvalues (EVs) from EFA suggest that marked changes in the hydration and secondary structure of BSA take place in the temperature ranges of 61-65 degrees C and 59-63 degrees C, respectively. In addition, the temperature of 71 degrees C marked in the EFA plots may correspond to the onset temperature of increase in the intermolecular beta-sheet structure.     

IKONOS image fusion process using steepest descent method with bi-linear interpolation

There are many image fusion processes to produce a high-resolution multispectral (MS) image from low-resolution MS and high-resolution panchromatic (PAN) images. But the most significant problems are colour distortion and fusion quality. Previously, we reported a fusion process that produced a1 m resolution IKONOS fused image with minimal spectral distortion. However, block distortion appeared at the edge of the curved sections of the fused image, which was reduced by performing the wavelet transformation as a post-process. Here, we propose an image fusion process using the steepest descent method with bi-linear interpolation, which can remove block distortion without using wavelet transformation. Bi-linear interpolation provides the proper initial values of the fused image, and then the steepest descent method produces the optimum results of the fusion process. These results achieve improvement on the spectral as well as spatial quality of a1 m resolution fused image when compared with other existing methods and remove block distortion completely.     

Nonintrusive appliance load monitoring based on integer programming

This paper presents a new nonintrusive appliance load monitoring technique based on integer programming. Nonintrusive appliance load monitoring is the problem of identifying the operating conditions of electric appliances in a house by observing only the overall load current and voltage. Since the overall load current is expressed as a superposition of the currents of the operating appliances, the monitoring problem can be formulated as an integer quadratic programming problem by expressing the operating conditions as integer variables. This problem is solvable with a sufficiently small computational burden thanks to the recent development of commercial software. The proposed method does not require relearning even when a new appliance is installed in the house. Furthermore, the proposed formulation is applicable to cases in which some appliance has multiple modes, and cases in which some appliances of the same type are operating simultaneously. The usefulness of the proposed technique is verified by experimental results. © 2010 Wiley Periodicals, Inc. Electr Eng Jpn, 174(2): 18–25, 2011; Published online in Wiley Online Library ( wileyonlinelibrary.com ). DOI 10.1002/eej.21040     

Hydrocracking of diphenylmethane and tetralin over bifunctional NiW sulfide catalysts supported on three kinds of zeolites

Hydrocracking reactions of diphenylmethane and tetralin were carried out over three kinds of zeolites with or without NiW sulfide to discuss the roles of catalytic bifunctionality in two types of hydrocracking reactions. It was found that strong acid sites were not needed for the hydrocracking of diphenylmethane, while the conversion of tetralin required relatively strong acid sites. Ultra-stable Y zeolite with strong acidity exhibited high hydrocracking activity for both reactions. In contrast, mordenite catalysts did not show high activity for either hydrocracking, though isomerization of tetralin and excess hydrocracking to gaseous products proceeded. The superior performances of ultra-stable Y zeolite in the tetralin hydrocracking were suggested to be related to the hydrogen transfer ability. In most cases, the loading of NiW sulfide enhanced catalytic activity. In the diphenylmethane hydrocracking, the role of NiW sulfide was found to supply active hydrogen to the hydrocracking active sites on zeolite and to prevent polymerization of benzyl cations. In the tetralin hydrocracking, the dehydrogenated products from tetralin were re-hydrogenated over NiW sulfide.     

Location of the egocenter in kinesthetic space.

The location of the egocenter in kinesthetic space was investigated in 4 experiments. Participants, with their eyes closed, adjusted a comparison stimulus after or while touching a standard in a transverse plane at the belly or shoulder level so that they perceived the line joining the comparison and the fixed standard as pointing directly at themselves. The mean location of the intersections of the obtained lines was taken as the location of the egocenter. The main results showed that the location of the kinesthetic egocenter depended on the hand or hands used for touching, the timing of touching, and the distance of the standard from the participant. Implications of these results were discussed in relation to models of the kinesthetic egocenter. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Simple digitally programmable attenuator using FG-MOSFETs

A very simple digitally programmable attenuator using FG-MOSFETs (floating-gate MOSFETs) is presented. HSPICE simulations of the circuit demonstrate a THD of less than -32 dB and a variable gain range of -13 to -31 dB with a supply voltage of ±1.5 V, load resistance of 10 kΩ and input signal of 3 V_p-p     

Chlorophyll assembled electrode for photovoltaic conversion device

Chlorophyll-a (Chl-a) assembled in hydrophobic domain by fatty acid with long alkyl hydrocarbon chain such as myristic acid (Myr), stearic acid (Ste) and cholic acid (Cho) modified onto nanocrystalline TiO₂ electrode is prepared and the photovoltaic properties of the nanocrystalline TiO₂ film by Chl-a are studied. Incident photon to current efficiency (IPCE) value at 660 nm in photocurrent action spectrum of Chl-a/Ste-TiO₂, Chl-a/Myr-TiO₂ and Chl-a/Cho-TiO₂ electrodes are 5.0%, 4.1% and 4.1%, respectively. Thus, the IPCE is maximum using Chl-a/Ste-TiO₂ electrode. From the results of photocurrent responses with light intensity of 100 mW cm⁻² irradiation or monochromatic light with 660 nm, generated photocurrent increases using Chl-a/Ste-TiO₂ electrode compared with the other Chl-a assembled TiO₂ electrodes. These results show that the hydrophobic domain formed by stearic acid with long alkyl hydrocarbon chain is suitable for fixation of Chl-a onto TiO₂ film electrodes and photovoltaic performance is improved using Chl-a onto Ste-TiO₂ film electrode.