went . fon wee a, “ ayes a a eS 4866, Radiochemical Analysis of ®Sr and 137¢s in Seawater Procedure Fe, Sr and Cs carriers were added to the water samples which were acidified with hydrochloric acid immediately after the samples were taken. - After the Ca and Sr carbonates were dis- +--gsolved in diluted HCl, the pH of the solution was adjusted to 8 with an ammonia solution in order to separate iron hydroxide by filtration. After EDTA was added to the filtrate as a masking agent for the majority of the Ca, 4g0dium carbonate was added to separate Sr with the remain| .ing free Ca. Precipitate was dissolved in diluted HNO3 then the fuming HNO method was used to separate ;8r.from Ca. 90Sr was counted with a low background, | yWindowless, gas flow counter. Nitric acid was added to -the filtrate from the carbonate and 137Cs was separated ,eby; the addition of microcrystalline ammonium molybdophos- £phate. 137Cs was counted with a r-ray spectrometer. —aeeres oc Bin OY "fodoa Tes,22° 6:Ld wy ! oo ae a 1: °F a ',0Meteorological Reserach Institute .. ter Pig.7. O - Sodium carbonate was added to separate the Ca and Sr -as carbonates. a Diaselved Oxygen ~ RadloactivityeDisagras REs at *Katsuko SARUHASHT: Yukio KATSURAGI and Teruko sANAZAdA

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