GPC Profile Change of Potato Starch with Extrusion Processing

Native potato starch (moisture content 15%) was treated by twin screw extruder under four operating conditions with varying barrel temperatures (110°C–230°C). These modified starch samples were compared to native and drum-dried starch. Starch sample solution for gel chromatography was prepared by the three methods (acidic, alkaline, and neutral methods). They were subjected to gel chromatography on Toyopearl HW-75, and some difference was found among the three gel chromatographic patterns obtained from the same starch solution. This discrepancy among GPC patterns suggests formation of some types of anhydro-bonds between chains of amylopectin and or amylose in the extrusion process. Elevating barrel temperature increases degree of depolymerization. The size of fragments formed with the treatment is bigger than that of oligosaccharides but smaller than that of amylose.     

Mechano-electrochemistry of a passive surface using an in situ micro-indentation test

Depassivation–repassivation of iron surfaces in boric–borate solutions were investigated by using the micro-indentation test. A pair of current peaks due to repair of the passive film following rupture of the film were observed during a series of indenter drives, i.e., loading and unloading of the indenter. The shape of the current peak depended on environmental conditions (conductivity and pH of the solution) and substrate conditions (mechanical processing history, alloyed element) as well as indentation conditions (repetition, maximum depth, and maximum load). Plastic deformation of the surface was accompanied by surface depassivation, while no depassivation occurred during the elastic deformation, indicating that the passive film on iron has a ductile property. The solution conditions did not affect the scale of depassivation but affected the rate of repassivation. Dislocations in the substrate made surface depassivation difficult but enhanced reactivity during the repassivation. The test also revealed that type-312L stainless steel has high corrosion resistance in a concentrated NaCl solution.     

Detail analysis of fusion neutronics benchmark experiment for iron

In order to specify the best nuclear data on iron, the fusion neutronics benchmark experiment on iron at Japan Atomic Energy Agency (JAEA)/Fusion Neutronics Source (FNS) was analyzed in detail with MCNP-4C and the latest nuclear data libraries, JENDL-3.3, FENDL-2.1, JEFF-3.1 and ENDF/B-VII.0. As a result, totally the calculation result with ENDF/B-VII.0 agreed with the measurement best, except that it underestimated the measured neutron flux above 10 MeV with the depth. It was noted that the calculation result with JENDL-3.3 overestimated the measured neutrons below a few keV. Through the DORT calculations based on the iron data in ENDF/B-VII.0, it was found out that the first inelastic scattering cross-section data of ⁵⁷Fe in JENDL-3.3 caused the overestimation.     

Friction-induced ultra-fine and nanocrystalline structures on metal surfaces in dry sliding

Sliding friction tests of pin-on-disc type were carried out for carbon steel, pure iron and pure copper, and the microstructure and hardness near the sliding surfaces were investigated in detail. It was found that patchy transfer layers with ultra-fine (<200 nm) structures were produced on the disc surfaces. Nanocrystalline grains of 30–50 nm were identified for carbon steel, and submicron sized grains of 100–150 nm were observed in pure copper. The thicknesses of the ultra-fine structures were in the range of 10–50 μm, depending on the specimen material, sliding speed and applied load. The hardness near the sliding surface of pure iron was increased compared with the matrix. It was suggested that the hardening was due to the very fine structure formed by severe plastic deformation, but not due to phase transformation caused by thermal effects.     

Influence of a fiber-network microstructure of paper-structured catalyst on methanol reforming behavior

A novel microstructured catalyst that consists of Cu/ZnO catalyst powders and ceramic fibers was successfully prepared using pulp fibers as a tentative matrix by a papermaking technique. As-prepared material, called a paper-structured catalyst, possessed porous microstructure with layered ceramic fiber networks (average pore size ca. 20 μm, porosity ca. 50%). In the process of methanol autothermal reforming (ATR) to produce hydrogen, paper-structured catalysts demonstrated both high methanol conversion and low concentration of undesirable carbon monoxide as compared with catalyst powders and pellets. The catalytic performance of paper-structured catalysts depended on the use of pulp fibers, which were added in the paper-forming process and finally removed by thermal treatment before ATR performance tests. Confocal laser scanning microscopy and mercury intrusion analysis suggested that the tentative pulp fiber matrix played a significant role in regulating the fiber-network microstructure inside paper composites. Various metallic filters with different average pore sizes, used as supports for Cu/ZnO catalysts, were subjected to ATR performance tests for elucidating the pore effects. The tests indicated that the pore sizes of catalyst support had critical effects on the catalytic efficiency: the maximum hydrogen production was achieved by metallic filters with an average pore size of 20 μm. These results suggested that the paper-specific microstructures contributed to form a suitable catalytic reaction environment, possibly by promoting efficient diffusion of heat and reactants. The paper-structured catalyst with a regular pore microstructure is expected to be a promising catalytic material to provide both practical utility and high efficiency in the catalytic gas-reforming process.     

Mobilization and Leaching of Natural and Water Dispersible Colloids in Aggregated Volcanic Ash Soil Columns

Colloid-facilitated transport enhances migration of strongly sorbing compounds (e.g., radionuclides, phosphorus, heavy metals) in soil and groundwater. Mobilization, transport and deposition of soil colloids are the underlying processes governing colloid-facilitated contaminant transport. Although significant progress has been made in simulating mobilization and transport/deposition of model colloids in different collector systems, it may be inadequate for the prediction of natural colloidal behavior in the subsurface. This study quantifies the leaching of natural volcanic ash soil colloids (NC) as well as the simultaneous transport of applied water dispersible soil colloids (WDC) in aggregated volcanic ash soil columns. Two water-saturated soil columns were irrigated with artificial irrigation water (AIW) at an intensity of 80 mm/hr for 60 hours. Two additional columns were irrigated at the same intensity, but a colloidal suspension of 5 mg/L was applied after 20 hours for a period of 20 hours. Effluent colloid concentrations were measured in each experiment. HYDRUS-1D was used for the simulation and estimation of colloid transport parameters. The results clearly showed different kinetics for applied colloid transport and natural colloid leaching. Transport of applied WDC followed first-order attachment kinetics, while the two-site equilibrium/kinetic model with equal fractions of equilibrium and kinetic sites best described the leaching of NC. Coupling these best model approaches well predicted the simultaneous leaching of natural and applied colloids, hereby providing a useful tool for the design of colloid-based in-situ soil remediation systems.     

Preliminary spectrum shifter design for intermediate energy nuclear data benchmark experiments with DT neutrons

Integral benchmark experiments with DT neutrons are not always sufficient for nuclear data benchmarking in the MeV region, below 10 MeV. A neutron spectrum shifter, which will be placed between a sample and a DT neutron source, is effective to moderate DT neutrons incident to the sample. In order to estimate effects of the spectrum shifter, the ratio of the contribution of 14 MeV neutrons in the leakage neutron and gamma-ray spectra was calculated with MCNP-4C for an experimental configuration at FNS of JAEA, Japan. The calculations were carried out for a Li₂TiO₃ sample with a Be, D₂O, or ⁷LiD spectrum shifter. It was found out that the Be shifter was superior to others and the Be shifter was effective to decrease the contribution of 14 MeV neutrons especially for secondary gamma-ray spectrum measurements.     

Functional binders for reversible lithium intercalation into graphite in propylene carbonate and ionic liquid media

Poly(acrylic acid) (PAA), poly(methacrylic acid) (PMA), and poly(vinyl alcohol) (PVA), which have oxygen species as functional groups, were utilized as a binder for graphite electrodes, and the electrochemical reversibility of lithium intercalation was examined in PC medium and ionic liquid electrolyte, lithium bis(trifluoromethanesulfonyl)amide dissolved in 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)amide (BMP-TFSA). Columbic efficiency of 75–80% with more than 300 mAh g^?1 was achieved upon first reduction/oxidation cycle in both electrolytes using these binding polymers, which were significantly improved in comparison to a conventional PVdF binder (less than 45% of columbic efficiency for the first cycle). For the graphite-PVdF electrode, co-intercalation and/or decomposition of PC molecules solvating to Li ions were observed by the electrochemical reduction, resulting in the cracking of graphite particles. In contrast, the co-intercalation and decomposition of PC molecules and BMP cations for the first reduction process were completely suppressed for the graphite electrodes prepared with the polymers containing oxygen atoms. It was proposed that the selective permeability of lithium ions was attained by the uniform coating of the graphite particles with PAA, PMA, and PVA polymers, because the electrostatic interaction between the positively charged lithium ions and negatively charged oxygen atom in the polymer should modulate the desolvation process of lithium ions during the lithium intercalation into graphite, showing the similar functions like artificial solid-electrolyte interphase.     

Determination of seventeen pesticide residues in agricultural products by LC/MS

Residues of 17 pesticides in agricultural products were determined by LC/MS with an atmospheric pressure chemical ionization (APCI) interface in both positive and negative ion modes. Pesticides were extracted with acetonitrile, and the extracts were cleaned-up with a primary and secondary amine (PSA) mini-column eluted with acetone-hexane (1:1). Rice, orange and potato were spiked with the 17 pesticides at 0.1 microgram/g and analyzed by the proposed method. The average recoveries of these pesticides usually ranged from 70 to 98% and the relative standard deviations were usually around 10%. These results suggested that LC/MS with APCI could be used to determine the residue levels of the 17 pesticides in these crops.     

Fracture behavior of niobium by hydrogenation and its application for fine powder fabrication

Fracture behavior of pure niobium (Nb) by several hydrogenation procedures has been investigated to elucidate the fundamental mechanisms of hydrogen pulverization, which can then be used to produce fine Nb powders with high purity. Concentric cracks and microcracks were introduced in recrystallized Nb specimens, leading to pulverization, when they absorb hydrogen enough to form a large volume of the face-centered orthorhombic β-NbH phase. This hydride phase exhibits anisotropic expansion of Nb lattice and embrittlement. Thus, the fracture of Nb plates occurs in the following sequence: hydrogen absorption, the formation of the ordered hydride phase, strain generation arising from the phase transformation, and crack nucleation and propagation. The authors also show that Nb powders less than 1 μm were prepared by hydrogenation and ball-milling at a temperature below 203 K, in which hydrogen was removed by dehydrogenation at above 724 K. Thus, fine and contamination-free Nb powders can be effectively fabricated by using hydrogenation, ball-milling, and dehydrogenation procedures.