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  • Author or Editor: M. Kinoshita x
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Abstract  

An analytical method for the determination of127I and129I in various environemntal samples has been developed. The method consists of the separation of iodine from the samples using a double layered quartz tube firing apparatus, post-irradiation purification of iodine, and measuring126I and130I by means of gamma spectrometry. The relative standard deviations of this method was less than 6%.

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Abstract  

For a realistic dose estimation, we derived the concentration factors (CF) of plutonium and americium for the field measurements of marine products and ambient coastal sea water.The distribution of the concentration ratios (CR) between the concentration in marine products and that in ambient sea water shows a lognormal distribution. The concentration factors of plutonium and americium which are derived as the geometric mean of CR values, are 231 and 67 for whitebait, 12 and 37 for flatfish, 350 and 220 for brown algea, 140 and 670 for shell fish, 27 and 130 for cephalopods, and 250 and 550 for crustaceans, respectively.

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Abstract  

An accurate and reliable method has been developed and routinely carried out for the sequential determination of239,240Pu and241Am in environmental samples. After suitable pretreatment.239,240Pu and241Am are separated from other elements by means of the anion exchange resin method. Americium-241 is purified by coprecipitation with calcium oxalate and then ion exchanged in mixed media of the mineral acid-methanol. In the analysis,242Pu (or236Pu) and244Cm are used as chemical yield monitors. The recoveries of the yield monitors in the analyses of some kinds of environmental samples were 7080% for plutonium and 7686% for curium. The concentration of239,240Pu in the coastal sea water were 7.022 Bq/l and that of241Am was 1.26.3 Bq/l. The mean concentrations of239,240Pu in the edible parts of the marine products ranged from 0.22 to 7.4 mBq/kg · fresh and those of241Am ranged from 0.11 to 2.6 mBq/kg · fresh.

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