Investigation report of geotechnical disaster on river area due to typhoon landfall three times on Okhotsk region,Hokkaido, Japan

For one week from August 17 to 23, 2016, three consecutive typhoons made landfall in Hokkaido for the first time on record. These typhoons and the front they stimulated brought record-breaking torrential rain over the eastern part of Hokkaido. To investigate the damage to grounds and rivers resulting from this rainfall, the Japan Society of Civil Engineers (JSCE) and the Japanese Geotechnical Society (JGS) formed a disaster research group to conduct an investigation. This report provides the results of the investigation into damage to the grounds of areas along the Tokoro River of the Okhotsk region, Hokkaido, that suffered from this tremendous and diverse disaster. Specifically, the report describes the situation of the levees which were broken and eroded by the overflowing water, the shape of the levee bodies, the levee body soil properties examined by observation of the sections, as well as the occurrence of sand boiling and air blows. The washout of road embankments as well as damage to road bridge mounting fills and abutment backfills were also investigated. The investigation has demonstrated the need to clarify the resistance of the abutment backfills and levee bodies to flowing water as well as the geotechnical predominant factors in order to clarify the mechanisms behind erosion and washout, the need to review new measures that allow for the scale of sand boiling and resultant changes in levee body stability, and the fact that the existing embankments were able to temporarily suppress the flooding water which had spilled over from the river. Furthermore, although it has been identified that the findings of a study on an embankment washout associated with a tsunami can be applied to measures taken against the overflowing water, it has also been found necessary to clarify the predominant geotechnical factors using model tests and to use a more sophisticated analytical approach to establish a geotechnical stability review as soon as possible in order to prevent the levees and embankments from being eroded and washed out due to overflowing water.     

Selective oxidation of ethane and propane over sulfated zirconia‐supported nickel oxide catalysts

The oxidative dehydrogenations of ethane and propane were investigated over a series of zirconia and nickel‐oxide supported on zirconia catalysts. It was found that zirconia, sulfated zirconia as well as NiO‐based zirconia catalysts showed high catalytic activities for oxidative dehydrogenation of ethane and propane. However, conversion and selectivity differed depending on the nature of the catalysts. Zirconia, sulfated zirconia (SZ) and their supported NiO catalysts showed high ethane conversions but lesser selectivities to olefins while NiO/Li₂ZrO₃ exhibited high selectivities to ethylene and propylene. Addition of an LiCl promoter in the NiO/SZ catalyst increased the catalytic activity and olefin selectivity, thus resulting in a higher olefin yield. In the oxidative dehydrogenations of ethane and propane NiO–LiCl/SZ exhibited 79% ethylene selectivity at 93% ethane conversion at 650 °C and 52% selectivity to propylene at 20% propane conversion at 600 °C, respectively. Characterization showed that the physico‐chemical properties of the catalysts determine the catalytic activity and selectivity. © 2001 Society of Chemical Industry     

Polymerization of styrene with a simple rare earth metal initiator

The catalytic activity in the polymerization of styrene has been examined using commercially available simple rare earth metal compounds such as Sm(OiPr)₃, Sm(acac)₃, Sm(OCOMe)₃, SmI₂(THF)₂ or SmCl₃ coupled with Et₃Al or methylaluminoxane (MAO). Among these compounds, the Sm(OiPr)₃/AlEt₃ system shows the highest catalytic activity, especially in the presence of a minor amount of toluene at 60 °C. The random copolymerization of styrene with methyl methacrylate suggests that the present polymerization proceeds with a radical polymerization mechanism. (C₅Me₅)SmCl₃Na(THF) and (C₅Me₅)SmCl₃Li(THF) systems exhibit relatively low catalytic activity, even in the presence of AlEt₃. © 2001 Society of Chemical Industry     

Structural analysis and transistor properties of hetero-molecular bilayers

We examined the film morphologies and transistor properties of hetero-molecular bilayer consisting of N, N’-dioctyl-3, 4, 9, 10-perylenedicarboximide (PTCDI-C₈) and quaterrylene. First, the structure and carrier conduction of PTCDI-C₈ films were studied, followed by an analysis of the carrier accumulation process in a PTCDI-C₈/quaterrylene hetero-bilayer transistor. Based on the displacement current measurement (DCM), we stress the potential of the hetero-bilayer for tuning carrier accumulation like carrier doping techniques in field-effect transistors.     

Area and volume effects on breakdown strength in liquid nitrogen

We measured dc and ac breakdown voltages in liquid nitrogen (LN ₂) with a sphere-to-plane electrode configuration. Experimental results revealed that the breakdown voltage in LN₂ did not increase monotonously but partially decreased as the sphere diameter increased at a constant gap length. Thus, the existence of the area and the volume effects on the breakdown voltage in LN₂ was verified quantitatively; the breakdown strength decreased when increasing the {SEA}₉₀ (90% stressed electrode area) and the {SLV}₉₀ (90% stressed liquid volume). By changing the experimental conditions, it was verified that both area and volume effects, having a mutual correlation, simultaneously lead to the degradation of the breakdown strength in LN₂. In order to examine the area and the volume effects for the larger {SEA}₉₀ and {SLV}₉₀, we also measured the breakdown voltage with a coaxial cylindrical electrode. It was concluded that the dc and ac breakdown strengths in LN₂ decreased as the {SEA}₉₀ and the {SLV}₉₀ increased varying widely from 10⁰ to 10⁵ mm² and from 10 ^-1 to 10⁵ mm³, respectively     

Simultaneous removal of NO/sub x/, SO/sub x/, and CO/sub 2/ at elevated temperature using a plasma-chemical hybrid process

In previous studies, the authors confirmed that the plasma-chemical combined hybrid process for controlling NO flue gas emission was extremely effective and economical in comparison with the conventional selective catalytic reduction (SCR) system and other technologies. In the present study, we carried out experiments on the simultaneous removal of NO/sub x/ and SO/sub x/ at elevated temperature using the plasma-chemical hybrid process. A series of experiments was performed to quantify all the reaction byproducts such as N/sub 2/O, CO, HNO/sub 2/, HNO/sub 3/, NO/sub 3//sup -/, and SO/sub 4//sup -/ to evaluate the simultaneous NO/sub x/ and SO/sub x/ removal efficiency. The oxidation from NO to NO/sub 2/ without decreasing NO/sub x/ concentration (i.e., minimum reaction byproducts) and with least power consumption is the key for the optimum operation of the plasma reactor. The produced NO/sub 2/ was totally converted to N/sub 2/ and Na/sub 2/SO/sub 4/ with Na/sub 2/SO/sub 3/ or Na/sub 2/S with and without NaOH using the barrier-type packed-bed plasma reactor followed by the packed-column chemical reactor. The NO/sub 2/ reduction was more effective for Na/sub 2/S than Na/sub 2/SO/sub 3/ but produces H/sub 2/S with Na/sub 2/S. For both cases at least five times the stoichiometric amount of chemicals were required for complete NO/sub 2/ reduction. Nearly 100% of NO/sub x/ and SO /sub 2/ and 40% Of CO/sub 2/ simultaneous removal were achieved with less than 5 ppm of N/sub 2/O and CO. The operating cost was less than 1/4 the SCR process. The additional SO/sub 2/ treatment system can be eliminated.     

Partial discharge inception characteristics under butt gap condition in liquid nitrogen/ PPLP/sup /spl reg// composite insulation system for high temperature superconducting cable

The partial discharge (PD) inception characteristics are studied in liquid nitrogen (LN/sub 2/)/polypropylene laminated paper (PPLP/sup /spl reg//) composite insulation system for high temperature superconducting (HTS) cable. Experimental results revealed that the magnitude of the initial PD increased as the PD inception electric field strength was increased, because the injected energy increased. Initial PD was generated at the first and third quadrant of applied AC voltage phase. The probability of initial PD at the positive and negative voltage phase was almost the same. The reason is because liquid nitrogen is a nonpolar molecule and we used symmetric electrode configuration with uniform electric field distribution. Finally, it was pointed out that PD inception electric field strength (PDIE) depended on the volume of the butt gap because of the increasing probability of weak points of electrical insulation, and PDIE linearly decreased with increasing stressed volume of the butt gap in the log-log scale.