New power consolidation-inversion-control system for faraday MHD generator

The authors propose a new power consolidation-inversion-control system for the Faraday MHD generator using the voltage source PWM inverters. The dc output power for each electrodes pair of the MHD generator is at first inverted into three-phase ac power by a voltage source PWM inverter, and then the ac powers are consolidated by transformers. The proposed system does not need such expensive equipment as an ac filter or phase modifier and can independently and simultaneously control the active and reactive powers provided to the electric power system. Numerical simulations of the whole system, including the Faraday MHD generator, the proposed power consolidation-inversion-control system, and the electric power system, show that the proposed system can stably and steadily transmit and control the electric power from the MHD generator to the electric power system. It is also confirmed that the proposed system can independently and simultaneously control the active and reactive powers and can be used as a fast power controller.     

Photo-induced radicals in glucose and cellobiose

Photo-induced radicals in glucose and cellobiose, the model compounds of cellulose molecule, were studied by ESR spectrometry. Very poor formation of radicals in glucose as compared to those in cellobiose was observed. However, a spectrum showing a singlet line was easily produced by the use of light involving shorter wavelengths. It was estimated to be due to the radical formed at the reducing C₁ position of glucose molecule. By paper chromatography, the photo-irradiated cellobiose was confirmed to split into glucose through scission of glucosidic bonds in the molecule. The ESR spectrum of the acid-hydrolyzed cellulose similar to that of the unhydrolyzed sample was a seven-line spectrum, but the relative signal intensity was here markedly low. This phenomenon seems to be caused by the reduction of amorphous portion in the samples due to acid hydrolysis. It was concluded that the glucosidic bonds in cellobiose and cellulose molecules are very active toward light and play an important role in the radical formation in photo-irradiated samples.     

Calculations for the availability of photoneutron using synchrotron radiation

The availability of the neutrons due to photonuclear reactions has been discussed by using synchrotron radiation with the beryllium targets. The superconducting wiggler with the magnetic field of approximately 10 T, which is installed into an 8 GeV class storage ring, can emit intense and high-energy photons to produce neutrons. By using MCNPX, the simulations were performed for the conceptual design of the neutron beamline to estimate the available intensity and to investigate the shield conditions. The results were discussed in comparison with other research reactors.     

Dibenzothiophene desulfurizing enzymes from moderately thermophilic bacterium Bacillus subtilis WU-S2B: purification, characterization and overexpression

The moderately thermophilic bacterium Bacillus subtilis WU-S2B desulfurized dibenzothiophene (DBT) at 50 degrees C through the selective cleavage of carbon-sulfur bonds. In this study, three enzymes involved in the microbial DBT desulfurization were purified and characterized. The first two enzymes, DBT monooxygenase (BdsC) and DBT sulfone monooxygenase (BdsA), were purified from the wild-type strain, and the last one, 2'-hydroxybiphenyl 2-sulfinic acid desulfinase (BdsB), was purified from the recombinant Escherichia coli overexpressing the gene, bdsB, with chaperonin genes, groEL/ES. The genes of BdsC and BdsA were also overexpressed. The molecular weights of BdsC and BdsA were determined to be 200 and 174 kDa, respectively, by gel filtration chromatography, suggesting that both enzymes had four identical subunits. BdsB had a monomeric structure of 40 kDa. The three enzymes were characterized and compared with the corresponding enzymes (DszC, DszA, and DszB) of mesophilic desulfurization bacteria. The specific activities of BdsC, BdsA, and BdsB were 84.2, 855, and 280 units/mg, respectively, and the latter two activities were higher than those of DszA and DszB. The heat stability and optimum temperature of BdsC, BdsA, and BdsB were higher than those of DszC, DszA, and DszB. Other enzymatic properties were investigated in detail.     

ESR study of the effect of ferric chloride on the photodegradation of model compound for polypropylene

In our previous article on the photodegradation of polypropyle (PP), the effect of ferric chloride (FeCl₃) accelerating the formation of peroxy radical and depressing the formation of alkyl radical were reported. In the present article, the influence of FeCl₃ on model compounds of PP was examined using electron spin resonance (ESR) spectrometry. The following compounds were employed as models of PP, including its irregular structures: 2-methylpentane (2-MP), 2,4-dimethylpentane (2,4-DMP), 2-methyl-4-pentanone (2-M4P), 2,6-dimethyl-4-heptanone (2,6-DM4H), 2-methyl-1-pentene (2-M1P), and tert-butylhydroperoxide (t-BuO₂H). FeCl₃ accelerated the formation of alkyl radicals for 2-MP and 2,4-DMP, alkyl and acyl radicals for 2-M4P and 2,6-DM4H, and alkyl radicals for 2-M1P. As no definite effect of FeCl₃ was observed for n-pentane and 2-octanone, FeCl₃ was assumed to attack saturated hydrocarbons, ketones at a tertiary carbon-hydrogen bond, and hydrocabons at an allylic hydroge, leading to easier photodegradations. FeCl₃ was also effective for the photodegradation of t-BuO₂H using λ >300 nm, so that FeCl₃ is believed to contribute also to the photodegradation of PP under the same irradation conditions. The catalytic effect of FeCl₃ in photodegradation seems to origirate in a redox reaction.     

On-chip cell sorting system using laser-induced heating of a thermoreversible gelation polymer to control flow

We have developed a microfabricated fluorescence-activated cell sorter system using a thermoreversible gelation polymer (TGP) as a switching valve. The glass sorter chip has Y-shaped microchannels with one inlet and two outlets. A biological specimen containing fluorescently labeled cells is mixed with a solution containing a thermoreversible sol-gel polymer. The mixed solution is then introduced into the sorter chip through the inlet. The sol-gel transformation was locally induced by site-directed infrared laser irradiation to plug one of the outlets. The fluorescently labeled target cells were detected with sensitive fluorescence microscopy. In the absence of a fluorescence signal, the collection channel is plugged through laser irradiation of the TGP and the specimens are directed to the waste channel. Upon detection of a fluorescence signal from the target cells, the laser beam is then used to plug the waste channel, allowing the fluorescent cells to be channeled into the collection reservoir. The response time of the sol-gel transformation was 3 ms, and a flow switching time of 120 ms was achieved. Using this system, we have demonstrated the sorting of fluorescent microspheres and Escherichia coli cells expressing fluorescent proteins. These cells were found to be viable after extraction from the sorting system, indicating no damage to the cells.     

Use of Ponkan mandarin peels as biosorbent for toxic metals uptake from aqueous solutions

Waste Ponkan mandarin (Citrus reticulata) peel was used as biosorbent to extract Ni(II), Co(II) and Cu(II) from aqueous solutions at room temperature. To achieve the best adsorption conditions the influence of pH and contact time were investigated. The isotherms of adsorption were fitted to the Langmuir equation. Based on the capacity of adsorption of the natural biosorbent to interact with the metallic ions, the following results were obtained 1.92, 1.37 and 1.31 mmol g(-1) for Ni(II), Co(II) and Cu(II), respectively, reflecting a maximum adsorption order of Ni(II)>Co(II)>Cu(II). The quick adsorption process reached the equilibrium before 5, 10 and 15 min for Ni(II), Co(II) and Cu(II), respectively, with maximum adsorptions at pH 4.8. In order to evaluate the Ponkan mandarin peel a biosorbent in dynamic system, a glass column was fulfilled with 1.00 g of this natural adsorbent, and it was fed with 5.00 x 10(-4)mol l(-1) of Ni(II) or Co(II) or Cu(II) at pH 4.8 and 3.5 ml min(-1). The lower breakpoints (BP(1)) were attained at concentrations of effluent of the column attained the maximum limit allowed of these elements in waters (>0.1 mg l(-1)) which were: 110, 100 and 130 bed volumes (V(effluent)/V(adsorbent)), for Ni(II), Co(II) and Cu(II), respectively. The higher breakpoints (BP(2)) were attained when the complete saturation of the natural adsorbent occurred, and the values obtained were: 740, 540 and 520 bed volumes for Ni(II), Co(II) and Cu(II), respectively.     

A variational method for geometric regularization of vascular segmentation in medical images

In this paper, a level-set-based geometric regularization method is proposed which has the ability to estimate the local orientation of the evolving front and utilize it as shape induced information for anisotropic propagation. We show that preserving anisotropic fronts can improve elongations of the extracted structures, while minimizing the risk of leakage. To that end, for an evolving front using its shape-offset level-set representation, a novel energy functional is defined. It is shown that constrained optimization of this functional results in an anisotropic expansion flow which is usefull for vessel segmentation. We have validated our method using synthetic data sets, 2-D retinal angiogram images and magnetic resonance angiography volumetric data sets. A comparison has been made with two state-of-the-art vessel segmentation methods. Quantitative results, as well as qualitative comparisons of segmentations, indicate that our regularization method is a promising tool to improve the efficiency of both techniques.     

Basis Translation Matrix between Two Isomorphic Extension Fields via Optimal Normal Basis

This paper proposes a method for generating a basis translation matrix between isomorphic extension fields. To generate a basis translation matrix, we need the equality correspondence of a basis between the isomorphic extension fields. Consider an extension field F_p^m where p is characteristic. As a brute force method, when p^m is small, we can check the equality correspondence by using the minimal polynomial of a basis element; however, when p^m is large, it becomes too difficult. The proposed methods are based on the fact that Type I and Type II optimal normal bases (ONBs) can be easily identified in each isomorphic extension field. The proposed methods efficiently use Type I and Type II ONBs and can generate a pair of basis translation matrices within 15 ms on Pentium 4 (3.6 GHz) when mlog₂ p = 160.     

Engineering of Lipid Nanoparticles by the Multifunctionalization of the Surface with Amino Acid Derivatives for the Neutralization of a Target Toxic Peptide

Protein affinity reagents (e.g., antibodies) are often used for basic research, diagnostics, separations, and disease therapy. Although a lot of “synthetic” protein affinity reagents have been developed as a cost-effective alternative to antibodies, their low biocompatibility is a considerable problem for clinical application. Lipid nanoparticles (LNP) represent a highly biocompatible drug delivery agent. However, little has been reported that LNP itself works as a protein affinity reagent in living animals. Here, LNP is engineered for binding to and neutralizing a target toxic peptide in living animals by multifunctionalization with amino acid derivatives. Multifunctionalized LNP (MF-LNP) is prepared using amino acid derivative-conjugated lipids. Optimized MF-LNP exhibits nanomolar affinity to the target toxic peptide and inhibits toxic peptide-dependent hemolysis and cytotoxicity. In addition, MF-LNP captures and neutralizes the toxic peptide after intravenous injection in the bloodstream; in addition, MF-LNP does not release the toxic peptide in the accumulated organ. These results reveal the potential of using LNP as a highly biocompatible protein affinity reagent such as an antidote.