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Tomita, Jumpei; Takeuchi, Erina
Applied Radiation and Isotopes, 150, p.103 - 109, 2019/08
Times Cited Count:14 Percentile:83.61(Chemistry, Inorganic & Nuclear)A rapid analytical method for determining Sr in urine samples (1-2 L) was developed to assess the internal exposure of workers in a radiological emergency. Strontium in a urine sample was rapidly separated by phosphate co-precipitation, followed by extraction chromatography with a tandem column of Pre-filter, TRU and Sr resin, and the Sr activity was determined by ICP-MS/MS. Measurement in the MS/MS mode with an O reaction gas flow rate 1 mL min showed no tailing of Sr at m/z = 90 up to 50 mg-Sr L. The interferences of Ge, Se and Zr at m/z = 90 were successfully removed by chemical separation. This analytical method was validated by the results of the analyses of synthetic urine samples (1.2-1.6 L) containing a known amount of Sr along with 1 mg of each of Ge, Se, Sr and Zr. The turnaround time for analysis was about 10 h, and the detection limit of Sr was approximately 1 Bq per urine sample.
Fujita, Hiroki; Nojima, Takehiro; Nagaoka, Mika; Osawa, Takahito; Yokoyama, Hiroya; Ono, Hironobu*
KEK Proceedings 2016-8, p.168 - 172, 2016/10
An automatic analysis system was developed to analyze Strontium-90 (Sr) radioactivity in environmental sample for 2013-2015. Various kinds of ashed environmental samples were used in performance tests of the automatic system. These tests were successful without any system trouble. However, Sr concentration had not been measured using the samples analyzed by the system. In this research, Sr concentration in seaweed sample was compared by between the system's analysis and worker's one. Moreover, the system was improved in each analysis process.
Nojima, Takehiro; Fujita, Hiroki; Nagaoka, Mika; Osawa, Takahito; Yokoyama, Hiroya; Ono, Hironobu*
KEK Proceedings 2015-4, p.111 - 115, 2015/11
Automatic strontium-90 analysis system was developed for environmental sample in this research. The system was successful to do wet ashing, chemical separation and ion exchange processes using robot, automatic heating system and so on. Hand-made control program can operate the system by itself.
Otosaka, Shigeyoshi; Amano, Hikaru; Ito, Toshimichi; Kawamura, Hideyuki; Kobayashi, Takuya; Suzuki, Takashi; Togawa, Orihiko; Chaykovskaya, E. L.*; Lishavskaya, T. S.*; Novichkov, V. P.*; et al.
Journal of Environmental Radioactivity, 91(3), p.128 - 145, 2006/00
Times Cited Count:20 Percentile:42.02(Environmental Sciences)Distributions of radionuclides (Sr, Cs and Pu) in seabed sediment in the Japan Sea were observed during 1998-2002. Observed inventories of anthropogenic radionuclides in sediment ranged 0.1-86 Bq m for Sr, 23-379 Bq m for Cs and 0.1-86 Bq m for Pu. In the deep part ( 2 km depth) of the western Japan Basin, Pu/Cs inventory ratios were larger than those in the central Yamato Basin although inventories of radionuclides were not different between basins. The higher Pu/Cs ratios in the western Japan Basin were derived by the production of Pu-enriched particle in the surface layer and effective sinking of particulate materials in this region. In the marginal Yamato Basin and the Ulleung Basin, both inventories and Pu/Cs ratios in sediment were larger than those in the central Yamato Basin. In the eastern/southern Japan Sea, it was suggested that the supply of particulate radionuclides by the TWC enhanced accumulation of radionuclides in this region.
Otosaka, Shigeyoshi; Ito, Toshimichi; Kawamura, Hideyuki; Kobayashi, Takuya; Suzuki, Takashi; Togawa, Orihiko
Dai-45-Kai Kankyo Hoshano Chosa Kenkyu Seika Rombun Shorokushu (Heisei-14-Nendo), p.77 - 78, 2003/12
no abstracts in English
Otosaka, Shigeyoshi; Aramaki, Takafumi*; Suzuki, Takashi; Kobayashi, Takuya; Ito, Toshimichi; Togawa, Orihiko; Chaykovskaya, E. L.*; Dunaev, A. L.*; Karasev, E. V.*; Novichkov, V. P.*; et al.
Proceedings of International Symposium on Radioecology and Environmental Dosimetry, p.390 - 395, 2003/10
Seabed sediments were collected at 22 stations in the Japan Sea, and anthropogenic radionuclides were measured in order to understand distributions and accumulation processes of these materials. Averaged concentrations of Cs in sediment in the Japan Basin and the Yamato Basin were 1.0 Bq/kg and 1.0 Bq/kg, respectively. Although there was no significant difference in mean Cs concentration between the Japan Basin and the Yamato Basin, distributions of radionuclides in these 2 basins showed different features. In the Japan Basin, the spatial variation of concentration of radionuclides was smaller than that at the Yamato Basin. At most stations in the Yamato Basin, significant concentrations of radionuclides were not detected, but remarkable large activities were observed at several stations in the Yamato Basin. For all radionuclides, the highest concentration was observed in the southeastern margin of the Yamato Basin. These results would suggest that there were different accumulation processes of radionuclides between the Japan Basin and the Yamato Basin.
Genka, Tsuguo; A.Mutalib*; H.I.Komala*; M.Ramli*; Adang.H.G.*; M.Sayad*; E.Sovilawati*; W.R.Suparna*
Kinrin Ajia Shokoku Niokeru Genshiryoku Anzen Kakuho Suijun Chosa Hokokusho, 0, p.254 - 266, 1996/02
no abstracts in English
Yamaguchi, Isoo; ; Morita, Yasuji; ; Shirahashi, Koichi; ; ; ; ; ; et al.
JAERI-Tech 94-030, 53 Pages, 1994/11
no abstracts in English
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JAERI-M 85-066, 22 Pages, 1985/06
no abstracts in English
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JAERI-M 84-140, 12 Pages, 1984/08
no abstracts in English
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Radioisotopes, 17(5), p.208 - 211, 1968/00
no abstracts in English
Fujita, Hiroki; Nojima, Takehiro*; Nagaoka, Mika; Osawa, Takahito; Ono, Hironobu*
no journal, ,
no abstracts in English