Development of a new loading test apparatus for microfocus X-ray CT and its application to the investigation of soil behavior surrounding driven open-section piles

In recent years, X-ray CT scanners with task-specific modifications, such as microfocus and/or a synchrotron, have been widely implemented in a variety of fields, including medical and industrial fields. Since microfocus X-ray CT systems enable the visualization of whole samples, and also yield a relatively high resolution of the region of interest in the sample, they are commonly utilized in the fields of soil mechanics and geotechnical engineering. This paper describes a novel loading test apparatus that is specifically designed for microfocus X-ray CT systems capable of performing loading tests to investigate soil behavior during the installation of driven open-section piles. The loading tests were designed to take the micro-level spatial resolution of microfocus X-ray CT systems into account. Digital image correlation (DIC) is subsequently implemented to analyze the obtained CT images, making it possible for measurements to be taken of the displacement fields in the ground following installation of the model pile. Finally, the versatility of this novel test apparatus is proof of its high potential for application in different types of loading tests.     

High-pressure viscosity prediction of di(2-ethylhexyl) phthalate and tricresyl phosphate binary mixtures using dielectric relaxation data

Dielectric permittivity and loss in di(2-ethylhexyl) phthalate and tricresyl phosphate binary mixtures were measured over a frequency range from 100 Hz to 1.5 MHz under high pressure. The mixtures showed single dielectric relaxation. The composite plots of the dielectric loss data showed one master curve and time–temperature–pressure superposition were applicable. The prediction of high-pressure viscosity was carried out from the change of dielectric relaxation time with temperature and pressure. The predicted results showed relatively good agreement with viscosity data obtained from a falling-sphere viscometer.     

Sources of nitrate and ammonium contamination in groundwater under developing Asian megacities

The status of nitrate (NO(3)(-)), nitrite (NO(2)(-)) and ammonium (NH(4)(+)) contamination in the water systems, and the mechanisms controlling their sources, pathways, and distributions were investigated for the Southeast Asian cities of Metro Manila, Bangkok, and Jakarta. GIS-based monitoring and dual isotope approach (nitrate delta(15)N and delta(18)O) suggested that human waste via severe sewer leakage was the major source of nutrient contaminants in Metro Manila and Jakarta urban areas. Furthermore, the characteristics of the nutrient contamination differed depending on the agricultural land use pattern in the suburban areas: high nitrate contamination was observed in Jakarta (dry fields), and relatively lower nutrients consisting mainly of ammonium were detected in Bangkok (paddy fields). The exponential increase in NO(3)(-)-delta(15)N along with the NO(3)(-) reduction and clear delta(18)O/delta(15)N slopes of NO(3)(-) ( approximately 0.5) indicated the occurrence of denitrification. An anoxic subsurface system associated with the natural geological setting (e.g., the old tidal plain at Bangkok) and artificial pavement coverage served to buffer NO(3)(-) contamination via active denitrification and reduced nitrification. Our results showed that NO(3)(-) and NH(4)(+) contamination of the aquifers in Metro Manila, Bangkok, and Jakarta was not excessive, suggesting low risk of drinking groundwater to human health, at present. However, the increased nitrogen load and increased per capita gross domestic product (GDP) in these developing cities may increase this contamination in the very near future. Continuous monitoring and management of the groundwater system is needed to minimize groundwater pollution in these areas, and this information should be shared among adjacent countries with similar geographic and cultural settings.     

Adhesion Properties of Nanometer-Thick Perfluoropolyether Films Confined Between Solid Surfaces: A Coarse-Grained Molecular Dynamics Study

Lubrication with thin liquid films is essential to ensure the tribological reliability of technologically advanced devices, such as micro-electro-mechanical systems and hard disk drives. However, the adhesion and friction properties of thin films and the underlying mechanism remain elusive due to our limited understanding of film structures and motions at the molecular scale. Here, we investigate the adhesion behavior of nanometer-thick perfluoropolyether (PFPE) films confined between two solid surfaces as a function of film thickness using coarse-grained molecular dynamics simulations. Consistent with typical experimental results, our simulations show that the adhesive force exerted by the PFPE films reaches a maximum and then decreases with increasing solid–solid spacing. The maximum adhesive force increases sharply for PFPE films thinner than 4 nm. When exhibiting the maximum adhesive force, PFPE films are slightly stretched within a solid–solid spacing a little larger than the initial film thickness and thereby show lower density than the original equilibrium density. Conventional theories of adhesion, which assume equilibrium density for liquid films, are not applicable in such case. Therefore, we construct a theoretical model that takes decreasing liquid density into account to discuss the underlying mechanism of the adhesive force exerted by nanometer-thick PFPE films on solid surfaces. We infer from the theoretical analyses that the maximum adhesive force originates mainly from solid–liquid interaction for thin films and liquid–liquid interaction for thick films.     

Development, Analysis, and Application of a Glass–Alumina-Based Self-Constrained Sintering Low-Temperature Cofired Ceramic

The effects of an inner constraint layer and alumina particles on the microstructure, strength, and shrinkage of the laminated low-temperature cofired ceramic (LTCC) green sheet were investigated. Alumina particles of several sizes were used in the inner-constraint layer in order to strengthen the LTCC substrate. Smaller alumina particles in the inner-constraint layer produced a substrate with a high bending strength. Sintering shrinkage in the x – y direction of the LTCC is related to the bending strength of the debinded alumina particle layer used for an inner-constraint layer. A larger pore size in the inner-constraint layer was found to increase the distance of the glass penetration from the glass–alumina layer into the inner-constraint layer. The total thickness of the constraint layer changes the shrinkage in the x – y direction and the bending strength.     

Si-C-O glass-like compound/exfoliated graphite composites for negative electrode of lithium ion battery

Two low molecular weight silicone compounds, a cyclic type having vinyl groups and a chain-type having Si-H bonds, a catalyst for curing, and a catalyst regulator were mixed. The mixture was impregnated into exfoliated graphite (EG) by sorption, and cured in air at 200 °C. By this process cross-linked silicone coatings were formed on graphite flakes. The composites of Si-C-O glass-like compounds and EG were synthesized by heat treatment of this precursor at 1000-1400 °C for 1 h in argon. The composites formed at 1000-1300 °C were amorphous by XRD and had practically the same chemical composition: Si 44-45, C 27-29, O 25-26, H < 0.5, all in mass%. The ²⁹Si MAS-NMR spectra indicated that the compound formed at 1000 °C was mainly composed of siloxane bonds and amorphous silica, whereas in the compound formed at 1300°C, Si-C bonds and amorphous silica were predominant. The insertion/extraction characteristics of lithium ions for the electrode prepared with composite:poly(vinylidene fluoride) = 90:10 mass% were examined in 1 mol L⁻¹ LiClO₄ solution of ethylene carbonate:diethyl carbonate = 50:50 vol%. High, 650-700 mA h g⁻¹, capacities and steady cycle performance at 50 mA g⁻¹ were achieved with the composites formed at 1250-1300 °C. Capacities of the composites formed at 1200 °C and lower were initially higher but decreased with increasing number of cycles. The composites formed at 1350 °C showed good cycle performance but the capacity was about 500 mA h g⁻¹ due to the formation of β-SiC. Except for the first cycle, the capacity-potential characteristics were similar to those of hard carbons and the coulomb efficiency was 95-100%. For all the composites the capacity was larger than that of graphite (372 mA h g⁻¹) in the range of 50-200 mA g⁻¹. Due to the large insertion capacity of the first cycle, the efficiency was low (60-70%) at first. By short-circuiting the working electrode to the lithium foil counter electrode for a certain period, the irreversible capacity of the first cycle was almost eliminated. It indicates that direct doping of lithium ions into composites is a promising way to increase the efficiency of the first cycle.     

Hydrogen adsorption and hydrogen evolution reaction on a polycrystalline Pt electrode studied by surface-enhanced infrared absorption spectroscopy

Hydrogen evolution reaction (HER) on a polycrystalline Pt electrode has been investigated in Ar-purged acids by surface-enhanced infrared absorption spectroscopy and electrochemical kinetic analysis (Tafel plot). A vibrational mode characteristic to H atom adsorbed at atop sites (terminal H) was observed at 2080-2095 cm⁻¹. This band appears at 0.1 V (RHE) and grows at more negative potentials in parallel to the increase in hydrogen evolution current. Good signal-to-noise ratio of the spectra enabled us to establish the quantitative relation between the band intensity (equivalently, coverage) of terminal H and the kinetics of HER, from which we conclude that terminal H atom is the reaction intermediate in HER and the recombination of two terminal H atoms is the rate-determining step. The quantitative analysis of the infrared data also revealed that the adsorption of terminal H follows the Frumkin isotherm with repulsive interaction.     

Femtosecond-laser-induced nanostructure formation and surface modification of diamond-like carbon film

This paper reports the pump and probe experiment for in situ reflectivity measurements in the femtosecond laser ablation that brings about nanoscale modification of diamond-like carbon (DLC) film. The characteristic reflectivity changes observed demonstrate that the formation of periodic nanostructure is preceded by a change in bonding structure of DLC in the ablation at low fluences. We have observed a coherent nonlinear wave-mixing signal that can resolve the ultrafast interaction processes for the nanoscale modification on the film surface. Based on the results obtained, a model of the interaction process is proposed.     

Influences of electroosmotic flows in nanopillar chips on DNA separation: Experimental results and numerical simulations

The various potential factors affecting the performance of nanopillar chips on DNA separation were investigated from the viewpoints of both numerical calculations and actual experiments. To yield higher performance and replace the conventional DNA separation techniques such as microchip electrophoresis, the phenomenon specific to the nanopillar chips should be deeply understood. In this paper, although various factors affecting the performance of the nanopillar chips are considered, we focused on the effect of electroosmotic flow, which is particularly noticeable in quartz-made nanopillar chips. High-resolution separation of DNA was realized when an electroosmotic flow was suppressed by simply using a higher concentration of buffer, but DNA separation failed in the presence of an electroosmotic flow. It was confirmed from the numerical simulations and the direct observations that the deformation of DNA band during the injection process was induced by electroosmotic flow and consequently led to a poor resolution.