Determination of radionuclide exchangeability in freshwater systems

被引:9
作者
Bunker, DJ
Smith, JT
Livens, FR
Hilton, J
机构
[1] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England
[2] CEH Dorset, Winfrith Technol Ctr, Dorchester DT2 8ZD, Dorset, England
关键词
freshwater sediments; radionuclide; exchangeability;
D O I
10.1016/S0048-9697(00)00701-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Two freshwater sediments were spiked with Co-57, Sr-85 and (CS)-C-134 and left for adsorption times ranging from 1 day to over 60 days. Following adsorption, the 'exchangeable' pool of each radionuclide was measured using ammonium acetate extractions and a sequential leach procedure (Tessier et al., 1979), and the results were compared. Exchangeabilty was found to depend upon the sediment, radionuclide, sorption time and the identity of extracting agent. All three radionuclides showed a shift with increasing adsorption time from regular exchange sites to sites which are sterically hindered, but a fixation within the sediment was only observed for Co-57 and Cs-134, With similar ammonium acetate extraction yields for both radionuclides. Misleading results were obtained during the sequential leach procedure due to redistribution and, therefore, the inclusion of a NH4+ leach after the MgCl2 extraction step was suggested. A mathematical model of element speciation was fairly successful at defining the 'exchangeable' fraction, suggesting that the chemically- and mathematically-defined fractions were similar. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:171 / 183
页数:13
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