Ultra-trace analysis of plutonium by thermal ionization mass spectrometry with a continuous heating technique without chemical separation.

Thermal ionization mass spectrometry (TIMS) with a continuous heating technique is known as an effective method for measuring the isotope ratio in trace amounts of uranium. In this study, the analytical performance of thermal ionization mass spectrometry with a continuous heating technique was investigated using a standard plutonium solution (SRM 947). The influence of the heating rate of the evaporation filament on the precision and accuracy of the isotope ratios was examined using a plutonium solution sample at the fg level.

Quantitative analysis of uranium in aqueous solutions using a semiconductor laser-based spectroscopic method.

A simple analytical method based on the simultaneous measurement of the luminescence of hexavalent uranium ions (U(VI)) and the Raman scattering of water, was investigated for determining the concentration of U(VI) in aqueous solutions. Both spectra were measured using a cw semiconductor laser beam at a center wavelength of 405 nm. The empirical calibration curve for the quantitative analysis of U(VI) was obtained by measuring the ratio of the luminescence intensity of U(VI) at 519 nm to the Raman scattering intensity of water at 469 nm.

Determination of plutonium content in high burnup pressurized water reactor fuel samples and its use for isotope correlations for isotopic composition of plutonium.

The content of plutonium isotopes in high burnup pressurized water reactor fuel samples was examined using both alpha spectrometry and mass spectrometry after anion exchange separation. The measured values were compared with results calculated by the ORIGEN-2 code. On average, the ratios (m/c) of the measured values (m) over the calculated values (c) were 1.

Thickness measurement of organic films using Compton scattering of characteristic X-rays.

An X-ray scattering method is presented for determining the thickness of an organic film placed on a steel substrate. The strong peaks of characteristic X-rays are taken as an advantage to measure the intensity of backscattered photons. It is shown that the intensity of Compton scattering of characteristic X-rays is proportional to film thickness, up to the thickness of 250 μm of acrylic adhesive layers.

Temperature dependence of fluorescence for EuCl3 in LiCl-KCl eutectic melt.

The fluorescence of EuCl(3) in LiCl-KCl eutectic melt according to temperature changes was investigated, and the spontaneous partial reduction of Eu(3+) to Eu(2+) at high temperature was confirmed by the fluorescence results. The fluorescence decreases when the temperature increases, and this was examined in detail. The studies of fluorescence provided information regarding the chemical and physical behavior of europium ions in the molten salt according to the temperature changes.

Isotope correlations for determining the isotopic composition of plutonium in high burnup pressurized water reactor (PWR) samples.

Correlations among the alpha activity ratios of (238)Pu/((239)Pu+(240)Pu), the alpha specific activities of Pu and the atom % abundances of Pu isotopes were derived for the plutonium samples obtained from high burnup fuel samples from pressurized water reactors. Using the alpha activity ratios of (238)Pu/((239)Pu+(240)Pu) determined by alpha spectrometry, the alpha specific activities of Pu as well as the atom % abundances of the plutonium isotopes in the unknown samples were calculated without depending on mass spectrometry. The calculated alpha specific activities of Pu agreed with those determined by experiment within 2%, and the atom % abundances of the Pu isotopes agreed within 4% for (238)Pu, 5% for (239)Pu, 7% for (240)Pu and 5% for (242)Pu, respectively.

Precipitation characteristics of uranyl ions at different pHs depending on the presence of carbonate ions and hydrogen peroxide.

This work studied the dissolution of uranium dioxide and precipitation characteristics of uranyl ions in alkaline and acidic solutions depending on the presence of carbonate ions and H2O2 in the solutions at different pHs controlled by adding HNO3 or NaOH in the solution. The chemical structures of the precipitates generated in different conditions were evaluated and compared by using XRD, SEM, TG-DT, and IR analyses together. The sizes and forms of the precipitates in the solutions were evaluated, as well.

Classification of materials for explosives from prompt gamma spectra by using principal component analysis.

Data from the elemental composition-ratios and experimental prompt gamma spectra of samples were used to develop suitable discriminant classes for suspect samples. The collected data and gamma spectra were applied to principal component analysis (PCA) to discriminate explosives from non-explosive materials.

Enhancement of the detection sensitivity for volatile organic compounds by using an annular type photoionization detector and a pre-concentration system.

Photoionization detector (PID) was developed for a sensitive on-site detection of trace amounts of volatile organic compounds (VOCs) based on an annular type ion collection electrode assembly. An ion collector with an annular geometry could detect more stable ion signals in the PID system when compared to the other types of ion collectors when an UV lamp of 10.6 eV was used as an ionization source.