Activation energy for diffusion of helium in water-saturated, compacted Na-montmorillonite

It is important to clarify the migration behavior of hydrogen gas dissolved in water-saturated, compacted bentonite, which is a promising material for geologic disposal of high-level waste and TRU waste disposal. The diffusion coefficients of helium, which can be detected under extremely low background conditions, in water-saturated, compacted Na-montmorillonite were determined as a function of temperature by a transient diffusion method. The activation energies for diffusion of helium were then obtained. The activation energies were from 6.9 ± 4.8 to 19 ± 2.8 kJ mol^− 1 and were regarded to be independent of dry density. The activation energies of helium in water-saturated Na-montmorillonite were roughly equal to those in bulk water, 14.9 kJ mol^− 1, and in ice, from 11 to 13 kJ mol^− 1. It is possible that helium diffuses not only in pore water but also in interlayer water.     

Accurate Isotopic and Concentration Analyses of Small Amounts of Pb Using Isotope Dilution Coupled with the Double Spike Technique

A new method has been developed for the simultaneous determination of Pb abundance and Pb isotopic composition with high precision and accuracy for small test portion masses by thermal ionisation mass spectrometry. In this method, a ²⁰⁵pb-²⁰⁴pb double spike is added to samples prior to the chemical separation of Pb, and the isotopic composition of the spike-sample mixture is determined rigorously by the double spike technique using a ²⁰⁷Pb-²⁰⁴Pb spike. The isotopic composition and concentration of Pb in the sample are then obtained by utilising the principle of isotope dilution. Using this technique, replicate determinations of Pb from NIST SRM 981 and GSJ JP-1 (peridotite; 0.07 μg g⁻¹ Pb) were performed. The measured concentration and isotopic data were identical, within uncertainty, to published data or to data that were determined independently in this study. The application of this method to U-Pb dating and the determination of the "initial" Pb isotopic composition was also tested. Lead isotopic compositions and the concentrations of Pb, Th and U were determined for a single batch of samples, through the addition of ²⁰⁵pb-²⁰⁴pb, ²³⁰Th and ²³⁵U spikes to samples prior to chemical separation. Also in these experiments, we confirmed that this routine gives accurate data for Pb, Th and U concentrations and Pb isotopic compositions.     

Seismic performance evaluation of non‐structural components: drywall partitions

As the first part of non‐structural component test series, interior drywall partitions are selected for an experimental program. This test series will cover non‐structural components that are significant in the economic losses in buildings subjected to seismic loading, namely interior drywall partitions, exterior cladding and window glasses, and ceilings. Four full‐scale drywall partitions with light‐gage steel stud framing were tested to observe damage in cyclic loading conditions. Effects of a door and an intersecting wall on the behaviour of drywall partition are studied. Damage was concentrated to perimeter regions where gypsum boards made contacts with ceiling, floor, or columns. Dynamic loading did not amplify the damage on a drywall partition over the damage observed from the quasi‐static test. Damage–repair cost relationships show that the repair cost reaches almost the initial cost under 2% radian interstorey drift. Copyright © 2006 John Wiley & Sons, Ltd.     

Chemical evidence for the origin of the cold water belt along the northeastern coast of Hokkaido

In the southwestern Okhotsk Sea, the cold water belt (CWB) is frequently observed on satellite images offshore of the Soya Warm Current flowing along the northeastern coast of Hokkaido, Japan, during summertime. It has been speculated that the CWB is upwelling cold water that originates from either subsurface water of the Japan Sea off Sakhalin or bottom water of the Okhotsk Sea. Hydrographic and chemical observations (nutrients, humic-type fluorescence intensity, and iron) were conducted in the northern Japan Sea and southwestern Okhotsk Sea in early summer 2011 to clarify the origin of the CWB. Temperature–salinity relationships, vertical distributions of chemical components, profiles of chemical components against density, and the (NO₃ + NO₂)/PO₄ relationship confirm that water in the CWB predominantly originates from Japan Sea subsurface water.