• Bulletin of the Korean Chemical Society
• /
• v.33 no.11
• /
• pp.3745-3748
• /
• 2012

This study presents a rapid and simple ${\alpha}$ source preparation method for a radioactive waste sample. The recovery of $^{239}Pu$, $^{232}U$ and $^{243}Am$ using a micro-coprecipitation method was over 95%. The ${\alpha}$-peak resolution of Pu and Am isotopes through the micro-coprecipitation method is enough to discriminate the Pu and Am isotopes from other Pu and Am isotopes. The determination of the Pu and Am isotopes using the micro-coprecipitation method was applied to the radioactive waste sample, so that the activity concentrations of the Pu and Am isotopes using the micro-coprecipitation method in the radioactive waste sample were similar to those using the electrodeposition method.

• Proceedings of the Korean Radioactive Waste Society Conference
• /
• 2005.06a
• /
• pp.248-254
• /
• 2005

This paper presents a quantitative method of sequential separation of $^{90}Sr,\;^{241}Am$ and Pu nuclides with an anion exchange resin and a Sr-Spec resin. The Pu isotopes were purified with an anion exchange resin. The americium and strontium fractions were separated from the matrix elements with an oxalate co-precipitation method. Americium fraction was separated from the strontium fraction with iron co-precipitation method and purified from lanthanides with anion exchange resin. Strontium-90 was purified from other hindrance elements with the Sr-Spec resin after oxalate co-precipitation. The measurement of Pu and Am isotopes was carried out by an ${\alpha}$-spectrometer. Strontium-90 was measured by a liquid scintillation counter. The radiochemical procedure of $^{90}Sr,\;^{241}Am$ and Pu nuclides investigated in this study has been validated by application to IAEA-Reference soils.

• Analytical Science and Technology
• /
• v.18 no.6
• /
• pp.469-474
• /
• 2005

This paper presents a quantitative method of sequential separation of $^{90}Sr$, $^{241}Am$ and Pu radionuclides with an anion exchange resin and a Sr-Spec resin. The Pu isotopes were purified with an anion exchange resin. The americium and strontium fractions were separated from the matrix elements with an oxalate co-precipitation method. Americium fraction was separated from the strontium fraction with iron co-precipitation method and purified from lanthanides with anion exchange resin. Strontium-90 was purified from other hindrance elements with the Sr-Spec resin after oxalate co-precipitation. The measurement of Pu and Am isotopes was carried out by an ${\alpha}$-spectrometer. Strontium-90 was measured by a liquid scintillation counter. The radiochemical procedure of $^{90}Sr$, $^{241}Am$ and Pu radionuclides investigated in this study has been validated by application to IAEA-Reference soils.

• Analytical Science and Technology
• /
• v.17 no.6
• /
• pp.514-519
• /
• 2004

Soil samples collected from around the BOMARC Missile Site were measured for their activity concentrations and isotopic ratios of Pu and Am isotopes with particle sizes. The activity concentrations of Pu and Am in the BOMARC soil were remarkably higher than the fallout levels, and the activities decreased nearly exponentially with an increasing particle size of the soil due to a decreasing surface area. The activity ratios of Pu-238 / Pu-239, 240, Pu-241 / Pu-239, 240 and Am-241 / Pu-239, 240 observed in the BOMARC soil were much lower than those attributed to the nuclear reprocess plants and the Chernobyl fallout. Also, the atomic ratio of Pu-240 / Pu-239 in the BOMARC soil was remarkably lower than the fallout value influenced by the nuclear weapons testing and the Chernobyl accident. The atomic ratio of Pu-240 / Pu-239 was so close to the value of the weapons grade Pu released from the crash of a B52 plane in the Thule of the Greenland, such that the Pu isotopes detected in the BOMARC soil could have originated from the weapons grade plutonium.

• Nuclear Engineering and Technology
• /
• v.50 no.1
• /
• pp.140-144
• /
• 2018

Isotopic analyses of plutonium and low-enriched uranium mixtures with particle sizes of $0.6-3.3{\mu}m$ were performed using thermal ionization mass spectrometry with a continuous heating method to verify its effectiveness for the accurate analysis of minor isotopes without sample pretreatment. The mixed particles used in this study were prepared from a mixed solution of plutonium (SRM 947) and uranium (U010, $^{235}U$ 1% enriched) reference materials. The isotope ratios for plutonium in the individual mixed particles, including $^{238}Pu/^{239}Pu$, $^{241}Pu/^{239}Pu$ as well as $^{240}Pu/^{239}Pu$, and $^{242}Pu/^{239}Pu$, were in good agreement with the certified values despite the isobaric interference of $^{238}U$ and $^{241}Am$. The isotope ratios for uranium in the mixed particles also agreed well with the certified values within the range of error. However, the isotope ratios for minor isotopes, such as $^{234}U$ and $^{236}U$, in the particles with diameters of less than approximately $1.8{\mu}m$ could not be measured because numbers of $^{234}U$ and $^{236}U$ atoms in analyzed particles are too low. These results indicate that thermal ionization mass spectrometry with a continuous heating method is applicable for the analysis of trace amounts of plutonium isotopes, including $^{238}Pu$ and $^{241}Pu$, despite the presence of the respective isobars $^{238}U$ and $^{241}Am$ in the microsamples.

• Proceedings of the Korean Radioactive Waste Society Conference
• /
• 2009.11a
• /
• pp.407-408
• /
• 2009

In this work, a quantitative method of the sequential separation of $^{90}Pu,\;^{90}Sr$ and $^{241}Am$ nuclides was developed in environmental soil samples using by an anion exchange resin connected with a Sr Spec resin. The sequential methods of Pu, $^{90}Sr$ and $^{241}Am$ nuclides can reduce analysis cost and time. With the sequential methodupdated in this study, the activity concentrations of $^{239,240}Pu,\;^{90}Sr$ and $^{241}Am$ in the IAEA reference materials were close to the reference values reported by the IAEA.

• Nuclear Engineering and Technology
• /
• v.39 no.5
• /
• pp.673-682
• /
• 2007

The contents of transuranic elements in high-burnup spent fuel samples were determined. The activity amounts of $^{238}Pu,\;^{239}Pu,\;^{240}Pu,\;^{241}Am,\;^{244}Cm\;and\;^{242}Cm$ were measured by alpha spectrometry using $^{242}Pu\;and\;^{243}Am$ as tracers, respectively. A spike addition method for $^{237}Np$ was established by an alpha and gamma spectrometry using $^{239}Np$ as a spike after the optimum conditions for the measurements of $^{237}Np\;and\;^{239}Np$, respectively, were obtained. A separation system using anion exchange chromatography and diethylhexylphosphoric acid extraction chromatography was applied for the separation of these elements. This method was applied to high-burnup spent nuclear fuel samples $(40{\sim}60GWD/MTU)$. The contents of the transuranic elements were compared with those by ORIGEN-2 code. Measurements and the calculations of the contents of the plutonium isotopes $^{238}Pu,\;^{239}Pu\;and\;^{240}Pu$ agreed to within 10% on average. The contents of $^{237}Np$ agreed to within approximately 5% except for one instance of a calculation, while those of $^{241}Am,\;^{244}Cm\;and\;^{242}Cm$ showed higher values by approximately 19%, 35% and 14% on average, respectively, compared to the calculations according to the burnup.

• Proceedings of the Korean Nuclear Society Conference
• /
• 2001.10a
• /
• pp.312-312
• /
• 2001

• Proceedings of the Korean Nuclear Society Conference
• /
• 2005.05a
• /
• pp.271-272
• /
• 2005

• Analytical Science and Technology
• /
• v.17 no.4
• /
• pp.302-307
• /
• 2004

Determination of actinides in the environmental sample requires separation of each element. This procedure is tedious and time consuming. And also, the detection limits of some nuclides using alpha spectrometry are rather higher. To overcome the lower detection limit and complicated separation procedure, a simple analytical technique for the determination of actinide isotopes in the environmental samples was developed and applied to IAEA and NIST reference sediment samples. For the separation of actinides from matrix, anion exchange resin and TRU-spec extraction chromatography resin were used and chemical yields were obtained using natural uranium, thorium, $^{242}Pu$ and $^{243}Am$ tracers. For overcoming the higher detection limits of U and Th in alpha spectrometry, neutron activation analysis was applied. Using combined method, the detection limit was increased about 10 times. The activity values of each isotope were consistent with the reference values reported by IAEA and NIST.