Mechanism of high energy absorption by foamed materials-foamed rigid polyurethane and foamed glass

Energy absorbability of foamed rigid materials, polyurethane and glass, was studied under a compressive load. The brittle materials were proved to absorb much energy in a manner similar to ductile materials. A mechanism for such high energy absorption was proposed, based on a fracture model in which crushing of cells initiates at the weakest cell followed by propagation to cells lying in the layer containing the weakest one and lying in a direction perpendicular to the compressive force; then the crushing propagates to another layer under the compressive force after the completion of the first layer crushing. In the period of one layer crushing, the strain energy stored in the period of compression prior to the crushing is temporarily released, and it is stored again in the period of compression after the crushing. The store and release of strain energy is assumed to be repeated until all cell layers are crushed. This mechanism of layer-by-layer crushing allows the cells to absorb strain energy repeatedly, and causes high energy absorption in the brittle foamed material. The calculated energy based on the mechanism agrees well with the observed one.     

Remarks on 4cst-elements for incompressible materials

Three-node triangular elements obtained from the intersecting diagonals of quadrilaterals are thoroughly investigated for the penalty method formulation of incompressible problems such as Stokes flow, Navier-Stokes flow, and small-deformation rubber elasticity. Equivalence of the present formulation to the one using 4-node quadrilateral isoparametric elements with selective reduced integration, is presented. Convergence, instability phenomenon, smoothing of the pressure distribution are studied together with decompositions into triangular elements.     

Decarboxylation of the 6-nitrobenzisoxazole-3-carboxylate anion catalyzed by cross-linked poly(4-vinylpyridinium) salts

Summary Catalysis of cationic polyelectrolytes for the decarboxylation of 6-nitrobenzisoxazole-3-carboxylate anion was studied in a buffer solution (pH=9.0). Cross-linked poly (4-vinylpyridinium) salts prepared from 4-vinylpyridine and , -dibromides were used as cationic catalysts. The cross-linked catalysts were found to accelerate markedly the decarboxylation in comparison with the linear water-soluble analogues. Effect of the polymer structure such as the length of (CH₂)_x linkages between positive charges on the catalytic activity was examined. It was suggested that the acceleration by the cross-linked polymer catalysts would be due to the hydrophobic microenvironment around the catalytic sites.     

Stable sound source tracking based on two updating algorithms

In this paper, we present a stable sound source tracking method based on two updating algorithm. In the method, an eigenvector spanning the signal subspace is updated by using the Projection Approximation Subspace Tracking (PAST) algorithm without the eigen‐decomposition of a correlation matrix. Then, a constrained minimization problem is formulated taking into account the stability, and the solution is determined successively by applying the Interior Point Least Square (IPLS) algorithm. As a result, stable tracking can be achieved without the peak search of a MUltiple SIgnal Classification (MUSIC) spectrum, which often requires enormous computational costs because many complex multiplying operations are involved. Several experimental results in real room environments have demonstrated the high accuracy and the low computational costs of the proposed method. © Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Distribution, diversity and regulation of alcohol oxidase isozymes, and phylogenetic relationships of methylotrophic yeasts

In this study, we attempted to classify the methylotrophic yeasts based on diversities of alcohol oxidase (AOD), i.e. zymogram patterns and partial amino acid sequences. According to zymogram patterns for AOD, members of the methylotrophic yeasts separate into two major lineages, one group involving strains having a single AOD and the other group, including Pichia methanolica, Candida pignaliae and C. sonorensis, showing nine AOD isozymes. Based on partial amino acid sequences of AOD, the methylotrophic yeasts could be divided into five groups, and this classification agrees mostly with grouping based on 26S domain D1/D2 rDNA nucleotide sequences, except for some strains. Moreover, the strains having AOD isozymes constitute one group with P. trehalophila, P. glucozyma and Pichia sp. strain BZ159, although these strains are divided into two types, based on amino acid sequences of second AODs. On the other hand, these AOD isozymes consist of two subunits; the first subunits are induced not only by methanol but also by glycerol and pectin, although the second subunits are mainly induced by methanol. These data indicate that AOD isozymes and second AOD genes distribute widely in several methylotrophic yeasts in the natural environment, and second AOD genes may have evolved as methylotrophic genes that can adapt to the environmental conditions of higher methanol concentrations.     

Efficiency of hydrogen internal combustion engine combined with open steam Rankine cycle recovering water and waste heat

A hydrogen internal combustion engine (HICE) wastes more heat, and producing nearly three times more water than a conventional engine. This paper describes the principle behind a novel waste heat recovery sub-system that exploits the water produced by an HICE as the working fluid for an open-cycle power generation system based on the Rankine cycle. Water from the HICE exhaust is superheated by the waste heat from the HICE and used to produce power in a steam expander. A fundamental thermodynamic model shows the contribution of the sub-system to the overall thermal efficiency of the HICE at various engine speeds, with and without a condenser. The results show that the condenser is not cost-effective and that the overall thermal efficiency with the proposed sub-system is 27.2% to 33.6%, representing improvements of 2.9% to 3.7%, at engine speeds of 1500 to 4500 rpm.     

Chlorine isotope fractionation during reductive dechlorination of chlorinated ethenes by anaerobic bacteria

Chlorine isotope fractionation during reductive dechlorination of trichloroethene (TCE) and tetrachloroethene (PCE) to cis-1,2-dichloroethene (cDCE) by anaerobic bacteria was investigated. The changes in the 37Cl/35Cl ratio observed during the one-step reaction (TCE to cDCE) can be explained by the regioselective elimination of chlorine accompanied by the Rayleigh fractionation. The fractionation factors (alpha) of the TCE dechlorination by three kinds of anaerobic cultures were approximately 0.994-0.995 at 30 degrees C. The enrichment of 37Cl in the organic chlorine during the two-step reaction (PCE to cDCE) can be explained by the random elimination of one chlorine atom in the PCE molecule followed by the regioselective elimination of one chlorine atom in the TCE molecule. The fractionation factors for the first step of the PCE dechlorination with three kinds of anaerobic cultures were estimated to be 0.987-0.991 at 30 degrees C using a mathematical model. Isotope fractionation during the first step would be the primary factor for the chlorine isotope fractionation during the PCE dechorination to cDCE. The developed models can be utilized to evaluate the fractionation factors of regioselective and multistep reactions.     

Isolation and characterization of benzene-tolerant Rhodococcus opacus strains

Twenty-two benzene-utilizing bacteria were isolated from soil samples. Among them, three isolates were highly tolerant to benzene. They grew on benzene when liquid benzene was added to the basal salt medium at 10--90% (v/v). Taxonomical analysis identified the benzene-tolerant isolates as Rhodococcus opacus. One of the benzene-tolerant isolates, designated B-4, could utilize many aromatic and aliphatic hydrocarbons including benzene, toluene, styrene, xylene, ethylbenzene, propylbenzene, n-octane and n-decane as sole sources of carbon and energy. Strain B-4 grew well in the presence of 10% (v/v) organic solvents that it was capable of using as growth substrates. Genetic analysis revealed the benzene dioxygenase pathway is involved in benzene catabolism in strain B-4. A deletion-insertion mutant defective in the benzene dioxygenase large and small subunits genes (bnz A 1 and bnz A 2) was as tolerant to organic solvents as the wild-type strain B-4, suggesting that utilization or degradation of organic solvents is not essential for the organic solvent tolerance of R. opacus B-4.