Combustion behavior and application of polyolefin‐based floor sheet laminated with Nylon‐6/clay nanocomposites film

Nanocomposites are potential materials that can be used to improve the flame resistance of polymers without the need for halogen‐based flame retardants. However, the nanocomposites cannot be used as the only raw material to produce final products as they are too expensive compared with low‐cost commodity plastics. Therefore, some types of polyolefin‐based floor sheet laminated with nanocomposites film were prepared for the cone calorimetric study to determine the suitable nanocomposites laminated structure for flame resistance. This study found that the polyolefin‐based floor sheet laminated with 200 µm Nylon‐6/montmorillonite nanocomposites film on the surface can reduce the HRR _max and the S significantly; other types of nanocomposites film‐laminated floor sheet were not able to reduce their flame resistance in comparison with the normal Nylon‐6 film‐laminated floor sheet. Meanwhile, based on the gas barrier performance, the higher aspect ratio of clay is assumed to contribute to the higher flame resistance of nanocomposites. Thus, the polyolefin‐based floor sheet laminated with Nylon‐6/sericite nanocomposites film on the surface was also prepared and examined in the cone calorimetric study. However, the Nylon‐6/sericite nanocomposites film surface‐laminated floor sheet did not cause a significant reduction in the HRR _max and S compared with the Nylon‐6/montmorillonite nanocomposites film surface‐laminated floor sheet. The grade determined according to the standard fire test and the mechanical properties of the Nylon‐6/montmorillonite nanocomposites film surface‐laminated floor sheet satisfied the requirements for floor sheets for Japanese railway vehicles. Copyright © 2010 John Wiley & Sons, Ltd.     

Catalyzed thermal decompositon of H2SO4 and production of HBr by the reaction of SO2 with Br2 and H2O

Decomposition of H₂SO₄ and production of HBr have been studied as a part of the research and development of the thermochemical hydrogen production from water. The catalytic activities of various metals and metal oxides on a porous alumina support were studied for the thermal decomposition of sulfuric acid in a fixed bed reactor. A Pt-Al₂O₃ catalyst gave a conversion of SO₃ close to the equilibrium at temperatures from 1073 to 1173 K and at a space velocity below 10 000 h^?1. It was also found that metal oxide catalysts such as CuO and Fe₂O₃ were as active as the Pt catalyst. To prepare SO₂-free HBr gas by the reaction between SO₂, Br₂ and H₂O, vapor-liquid equilibrium determinations for SO₂/Br₂/HBr/H₂SO₄/H₂O system were carried out at 298 K under atmospheric pressure. The unconverted SO₂ can be effectively removed by contacting the effluent gases with a HBr saturated aqueous solution containing an excess of Br₂.     

A model of carbon ion interactions in water using the classical trajectory Monte Carlo method

In this paper, model calculations for interactions of C(6+) of energies from 1 keV u(-1) to 1 MeV u(-1) in water are presented. The calculations were carried out using the classical trajectory Monte Carlo method, taking into account the dynamic screening of the target core. The total cross sections (TCS) for electron capture and ionisation, and the singly and doubly differential cross sections (SDCS and DDCS) for ionisation were calculated for the five potential energy levels of the water molecule. The peaks in the DDCS for the electron capture to continuum and for the binary-encounter collision were obtained for 500-keV u(-1) carbon ions. The calculated SDCS agree reasonably well with the z(2) scaled proton data for 500 keV u(-1) and 1 MeV u(-1) projectiles, but a large deviation of up to 8-folds was observed for 100-keV u(-1) projectiles. The TCS for ionisation are in agreement with the values calculated from the first born approximation (FBA) at the highest energy region investigated, but become smaller than the values from the FBA at the lower-energy region.     

The Calcium Phosphate Matrix of FGF-2-Apatite Composite Layers Contributes to Their Biological Effects

The purpose of the present study was to fabricate fibroblast growth factor (FGF)-2-apatite composite layers on titanium (Ti) pins in one step at 25 °C using a supersaturated calcium phosphate (CaP) solution, and to evaluate the physicochemical characteristics and biological effects of the coated Ti pins compared with coated Ti pins fabricated at 37 °C. Ti pins were immersed in a supersaturated CaP solution containing 0.5, 1.0, or 2.0 µg/mL FGF-2 at 25 °C for 24 h (25F0.5, 25F1.0, and 25F2.0) or containing 4.0 µg/mL FGF-2 at 37 °C for 48 h (37F4.0). Except for the 25F0.5, the chemical compositions and the mitogenic activity levels of FGF-2 of the composite layers formed by these two methods were similar, except for the Ca/P molar ratio, which was markedly smaller at 25 °C (1.55–1.56 ± 0.01–0.02, p = 0.0008–0.0045) than at 37 °C (1.67 ± 0.11). Thus, either the apatite was less mature or the amount of amorphous calcium phosphate was higher in the composite layer formed at 25 °C. In vivo, the pin tract infection rate by visual inspection for 37F4.0 (45%) was lower than that for 25F1.0 (80%, p = 0.0213), and the rate of osteomyelitis for 37F4.0 (35%) was lower than that for 25F0.5 (75%, p = 0.0341). The extraction torque for 37F4.0 (0.276 ± 0.117 Nm) was higher than that for 25F0.5 (0.192 ± 0.117 Nm, p = 0.0142) and that for 25F1.0 (0.176 ± 0.133 Nm, p = 0.0079). The invasion rate of S. aureus for 37F4.0 (35%) was lower than that for 25F0.5 (75%, p = 0.0110). On the whole, the FGF-2-apatite composite layer formed at 25 °C tended to be less effective at improving fixation strength in the bone-pin interface and resisting pin tract infections. These results suggest that the chemistry of the calcium phosphate matrix that embeds FGF-2, in addition to FGF-2 content and activity, has a significant impact on composite infection resistance and fixation strength.     

An atomistic study of grain boundary stability and crystal rearrangement using molecular dynamics techniques

The stability of grain boundaries (GBs) and the dynamic behavior of atoms in the boundary region are investigated from an atomistic standpoint. Symmetric and non-symmetric GBs are constructed using an fcc configuration, and the GB energy is calculated as a function of the misorientation angles using a Lennard-Jones-type interatomic potential. Several specific angles are revealed to exhibit cusp-shaped low values. The effect of atomic relaxation at the GB is then simulated, showing a decrease in the GB energy. Changes in the morphology of a grain embedded in a bulk single crystal are also simulated. Using both a square-grain and a circular-grain model, the following results are obtained. In models with small misorientation angles, the grain changes orientation and the GB vanishes. When the orientations are initially stable, no change in the grain is observed. However, in models with non-stable orientations, local stabilization occurs by a rearrangement of the atoms around the GB, and the shape of the grain is transformed. Finally, a similar simulation is carried out at a high temperature, and this reveals that grain contraction occurs even in models that are stable at a low temperature, and that the grain eventually disappears.     

Distribution of macrolides, sulfonamides, and trimethoprim in tropical waters: ubiquitous occurrence of veterinary antibiotics in the Mekong Delta

We investigated the distributions of 12 antibiotics (viz., sulfonamides, macrolides, and trimethoprim) in the water from the Mekong Delta, Vietnam, and compared them with those in the Tamagawa River, Japan. In Vietnam, only a few antibiotics (viz., sulfamethoxazole, sulfamethazine, trimethoprim, and erythromycin-H2O) were detected in the river and canals from urban and rural sites, at concentrations of 7-360 ng/L. This contrasts with the results from the Japanese urban river, where more antibiotics (sulfamethoxazole, sulfapyridine, trimethoprim, erythromycin-H20, azithromycin, clarithromycin, and roxithromycin) were detected at concentrations ranging from 4to 448 ng/L. The concentrations of sulfonamides in the Mekong Delta were comparable to those in the Tamagawa River, whereas macrolide concentrations were lowerthanthose in the Tamagawa River. The ubiquitous occurrence of sulfamethazine, used as a veterinary medicine, in the waters in Vietnam at relatively high concentrations (15-328 ng/L) was unique. Extremely high concentrations of sulfamethazine [(18.5-19.2) x 10(3) ng/L] were detected in pig farm wastewaters, and relatively high concentrations were observed in canals near chicken and pig farms. All these data suggested the potential utility of sulfamethazine as a molecular marker of livestock-source contamination. The present study demonstrated widespread inputs of veterinary medicines to waters in Vietnam.     

Three-dimensional observation of SiO2 hollow spheres with a double-shell structure using aberration-corrected scanning confocal electron microscopy

Optical sectioning using scanning confocal electron microscopy (SCEM) is a new three-dimensional (3D) imaging technique which promises improved depth resolution, particularly for laterally extended objects. Using a stage-scanning system to move the specimen in three dimensions, two-dimensional (2D) images sliced from any plane in XYZ space can be obtained in shorter acquisition times than those required for conventional electron tomography. In this paper, a double aberration-corrected SCEM used in annular dark-field mode was used to observe the 3D structure of SiO(2) hollow spheres fabricated by a carbon template method. The double-shell structure of the sample was clearly reflected in both XY- and XZ-sliced images. However, elongation along the optical axis was still evident in the XZ-sliced images even when double aberration correctors were used. Application of a deconvolution technique to the experimental XZ-sliced images reduced the elongated shell thicknesses of the SiO(2) sphere by 40-50% and the selectivity of information at a certain sample depth was also enhanced. Subsequently, 3D reconstruction by stacking the deconvoluted slice images restored the spherical surface of a SiO(2) sphere.     

Identification of fungi using DNA sequences: an approach to identify Fusarium species isolated from domestic unpolished rice

Molecular approaches are being developed to provide for the rapid and objective identification of fungi. We attempted the identification of Fusarium species by a genetic analysis to validate practically the utility of a molecular approach for fungal identification and to reveal its limitations, and sequenced three regions, the 5' end of the 28S rRNA gene (D2 region) and the internal transcribed spacer 1 and 2 (ITS1 and ITS2) regions, in the rRNA genes. The DNA sequences of 38 Fusarium strains isolated from domestic unpolished rice were compared for similarity with entries in the GenBank. Based on this comparison, it was estimated that all these three regions, as a minimum, must be compared with the database to identify Fusaria at the species level. According to the combinations of sequences in the three regions, the 38 isolates were classified into 13 groups. Out of the 13 groups, 6 groups (20 isolates in total) could be identified as definite species based only on the sequence data. For the other 6 groups (17 isolates in total), candidate species were limited on the basis of the sequence similarity, and then the isolates were identified at the species level with the aid of morphology. Only one isolate could not be identified. These results verified that DNA sequence comparison with the GenBank database is useful for the identification of Fusarium species.     

Physicochemical properties of cross-linked poly-gamma-glutamic acid and its flocculating activity against kaolin suspension

Cross-linked poly-gamma-glutamic acid (C-L gamma-PGA) was prepared with gamma-PGA irradiated with gamma-ray at various kGy values. The physicochemical properties including viscosity and water absorption capacity were compared between C-L gamma-PGA and several typical flocculating agents. The viscosity of C-L gamma-PGA increased with the dose of gamma-irradiation, although the water absorption capacity of C-L gamma-PGA did not, which showed a maximum of 1005.6 ml/g at 20 kGy. Flocculating activity against kaolin suspension was not observed for any of the test compounds when used singly. However, the activity of C-L gamma-PGA markedly increased following the addition of polyaluminum chloride. The activity increased with temperature up to 80 degrees C and remained at 80 degrees C of heat pretreatment for 1 h, but did not at more than 50 degrees C of heat pretreatment for 24 h. The activity was also observed within a pH range of 4.5-10.0. Both the water absorption capacity and flocculating activity of C-L gamma-PGA decreased in parallel with increasing NaCl concentration, suggesting that the flocculating activity of C-L gamma-PGA was associated with its water absorption capacity, rather than viscosity. An investigation of the effects of various cations on the flocculating activity of C-L gamma-PGA showed that only trivalent cations had a synergistic effect. The mechanism of C-L gamma-PGA flocculating activity is discussed based on the results of preliminary experiments.