共 50 条
The availability of plutonium and americium in Irish Sea sediments for re-dissolution
被引:31
|作者:
McDonald, P
[1
]
Batlle, JVI
[1
]
Bousher, A
[1
]
Whittall, A
[1
]
Chambers, N
[1
]
机构:
[1] Westlakes Sci Consulting Ltd, Environm Sci, Moor Row CA24 3LN, Cumbria, England
关键词:
plutonium;
americium;
actinide;
re-dissolution;
speciation;
Irish Sea;
Sellafield;
D O I:
10.1016/S0048-9697(00)00771-3
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
The availability of plutonium and americium, for re-dissolution from offshore sediments into Irish Sea water, has been examined. Sediments collected from the mud-patch near the Cumbrian coast were characterized in terms of spatial location, particle size, partitioning of radionuclides with respect to physico-chemical bonds and availability of actinides for release into seawater. Sequential extraction investigations revealed that plutonium was predominantly associated with strongly bound sesquioxide and organic complex fractions. Americium was associated mainly with the organic complex fraction, but a significant fraction was in carbonate form. Sediment/water re-dissolution experiments with and without stirring were compared to simulate the effect of disturbing bed sediment. After 1 week, neither set of re-dissolution data provided significant trends between dissolved activity and time. Stirred systems appeared to release 2.5 times more plutonium and americium into seawater than unstirred systems. Measured Pu-239,Pu-240 and Am-241 distribution coefficients (K-d values) were both typically approximately 10(5) 1 kg(-1). Am-241 K-d values are an order of magnitude lower than previously reported for the north-eastern Irish Sea, but similar to western Irish Sea values. Overall, the fractions of plutonium and americium available for re-dissolution from bed sediment are very low at < 0.1%, with proportionally more plutonium being released than americium. These findings lend further support for the extrapolation of laboratory-derived information to environmental conditions. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:109 / 123
页数:15
相关论文