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Miyamoto, Yutaka; Saito, Yoko; Magara, Masaaki; Usuda, Shigekazu
Journal of Radioanalytical and Nuclear Chemistry, 255(3), p.553 - 557, 2003/03
Times Cited Count:4 Percentile:31.76(Chemistry, Analytical)To investigate the effect of weather on the composition of the dust and the possible origin of the dust, the elemental composition airborne dust was determined by INAA. The analyzed elements could be classified into 3 groups by the variation of concentration in the samples. The difference in concentration pattern may reflect the effect of rainfalls.
Hashimoto, Kazuyuki; Matsuoka, Hiromitsu; Uchida, Shoji*
Journal of Radioanalytical and Nuclear Chemistry, 255(3), p.575 - 579, 2003/03
Times Cited Count:40 Percentile:91.58(Chemistry, Analytical)The emitter
Lu is a promising therapeutic radioisotope for the treatment of cancer. It has a half-life of 6.73 days and maximum
energy of 498 keV, resulting in a short range of radiation in tissue. The decay is accompanied by the emission of low energy
-radiation with
= 208 keV (11.0%) and 113 keV (6.4%) suitable for simultaneous imaging. Lutetium-177 can be usually produced at nuclear reactors with high yield and high specific radioactivity by the
Lu(n,
)
Lu reaction. However, radioisotopes with higher specific radioactivity are required in the field of radioimmunotherapy using labeled monoclonal antibodies. Thus, an alternative production route, namely the
Yb(n,
)
Yb
Lu process was studied to produce no-carrier-added (nca)
Lu in this work. The radiochemical separation of the nca
Lu from the macroscopic ytterbium target was investigated by means of reversed-phase ion-pair HPLC. The nca
Lu was obtained in radiochemical pure form with a separation yield of 80%.
Nagao, Seiya*; Fujitake, Nobuhide*; Kodama, Hideki*; Matsunaga, Takeshi; Yamazawa, Hiromi
Journal of Radioanalytical and Nuclear Chemistry, 255(3), p.459 - 464, 2003/03
Times Cited Count:7 Percentile:46.03(Chemistry, Analytical)no abstracts in English
Watanabe, Satoshi; Ishioka, Noriko; Sekine, Toshiaki; Osa, Akihiko; Koizumi, Mitsuo; Shimomura, Haruhiko*; Yoshikawa, K.*; Muramatsu, Hisakazu*
Journal of Radioanalytical and Nuclear Chemistry, 255(3), p.495 - 498, 2003/03
Times Cited Count:11 Percentile:59.69(Chemistry, Analytical)no abstracts in English
Saito, Yoko; Miyamoto, Yutaka; Magara, Masaaki; Sakurai, Satoshi; Usuda, Shigekazu
Journal of Radioanalytical and Nuclear Chemistry, 255(2), p.341 - 345, 2003/02
Times Cited Count:4 Percentile:31.76(Chemistry, Analytical)no abstracts in English
Arisaka, Makoto*; Kimura, Takaumi; Suganuma, Hideo*; Yoshida, Zenko
Journal of Radioanalytical and Nuclear Chemistry, 255(2), p.385 - 389, 2003/02
Times Cited Count:5 Percentile:36.91(Chemistry, Analytical)no abstracts in English
Ueno, Takashi; Nagao, Seiya; Yamazawa, Hiromi
Journal of Radioanalytical and Nuclear Chemistry, 255(2), p.335 - 339, 2003/02
Times Cited Count:19 Percentile:77.44(Chemistry, Analytical)To evaluate the migration of radionuclides to the ground surface, deposition was collected from 1993 to 2001 with basin set up at Japan Atomic Energy Research Institute at Tokai-mura. Monthly basin samples were evaporated to dryness to obtain residual samples.These samples were measured by a well type Ge detector for natural and fallout radionuclide. These monthly depositions showed a clear seasonal variation with peaks in the early spring from February to April, and also in May in some years. The depositions of K and
Cs have good correlation with the dry weight of deposited material, the depositions of
Be and
Pb showed much lower correlation coefficients. This difference in the correlation coefficient between these two groups of radionuclides can be attributed to the difference in the originating processes. These features in the concentration are thought to be caused by the difference in mechanism and location of origination, which would result in difference in the contributing particle size, and hence by the difference in the transport and deposition processes.
Yonezawa, Chushiro; Matsue, Hideaki; Yukawa, M.*
Journal of Radioanalytical and Nuclear Chemistry, 255(1), p.105 - 109, 2003/01
Times Cited Count:5 Percentile:36.91(Chemistry, Analytical)no abstracts in English
Guo, J.; Atarashi-Andoh, Mariko; Amano, Hikaru
Journal of Radioanalytical and Nuclear Chemistry, 255(1), p.223 - 229, 2003/01
Times Cited Count:7 Percentile:46.03(Chemistry, Analytical)Soil organic matter content, C,
C and
Cs radioactivity were determined in 3 undisturbed forest soil profiles in Ibaraki prefecture, Japan to estimate
C migration in surface environment. The
Cs data illustrate that no disturbance has occurred during past years in 3 soil profiles. The peak values are observed in the top 10 cm of the soil profiles.
C activities were determined with fast bomb combustion-liquid scintillation counting method.
C determination shows that
C also has peak values in the top 10 cm of the soil profiles ascribed to the highest bomb
C level in 1960's.
C values continuously decreased with increasing soil depth. Enrichment of deeper soils in isotope ratio probably results from discrimination against
C during mineralization and loss of isotopically lighter carbon from soils due to root uptake, leaching etc.It shows that
C is an excellent indicator of soil carbon turnover and belowground process.
Matsue, Hideaki; Yonezawa, Chushiro
Journal of Radioanalytical and Nuclear Chemistry, 255(1), p.125 - 129, 2003/01
Times Cited Count:8 Percentile:50.12(Chemistry, Analytical)no abstracts in English
Amano, Hikaru; Onuma, Yoshikazu*
Journal of Radioanalytical and Nuclear Chemistry, 255(1), p.217 - 222, 2003/01
Times Cited Count:8 Percentile:50.12(Chemistry, Analytical)no abstracts in English
Hatsukawa, Yuichi; Toh, Yosuke; Oshima, Masumi; Hayakawa, Takehito; Shinohara, Nobuo; Kushita, Kohei; Ueno, Takashi; Toyoda, Kazuhiro*
Journal of Radioanalytical and Nuclear Chemistry, 255(1), p.111 - 113, 2003/01
Times Cited Count:12 Percentile:62.55(Chemistry, Analytical)no abstracts in English