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钚的形态对玛雅克土壤中分配系数的影响。

The impact of Pu speciation on distribution coefficients in Mayak soil.

作者信息

Skipperud L, Oughton D, Salbu B

机构信息

Laboratoryfor Analytical Chemistry, Agricultural University of Norway, Aas.

出版信息

Sci Total Environ. 2000 Aug 10;257(2-3):81-93. doi: 10.1016/s0048-9697(00)00443-5.

Abstract

To assess the long-term consequences when radionuclides are released into the environment, information on the source term, transport and transformation processes, interaction with soils (KD) and biological uptake (CF) is needed. Among the artificial radionuclides released to the environment by nuclear activities, the transuranium elements are a major concern, due to very long half-lives and their accumulation in bone as well as high radiotoxicity. Plutonium has been produced in greater quantity than other transuranic elements, however, environmental assessments are complicated by the complex environmental behaviour. Physico-chemical forms of Pu will determine the interactions with soils and, thus, the degree to which soils can act as a sink or a potential diffuse source of contaminants. In the present work, dynamic tracer experiments have been performed where different Pu-species are added to a 'Mayak soil-rainwater system' to obtain information on KD values. After a defined contact time, the samples where then sequentially extracted and results are used in a dynamic box model to estimate interaction and fixation rates. The interaction of all Pu-species with soils seems to be rapid and follows a two-step reaction. Up to contact times of a few weeks, the KD for Pu(III,IV) (730 +/- 240 l/kg) is approximately one order of magnitude higher than for Pu(V,VI) (90 +/- 20 l/kg) and Pu(III,IV)-organic (40-60 l/kg). After 3 months contact time, the KD in only the two organic-bound Pu-species were significantly lower. This shows that the initial association with the soil is dependent on the Pu-species in the rainwater. After only 1 h of contact, between 33 and 40% of the plutonium was strongly bound to the soil components, i.e. only extractable with strong HNO3. The extraction of soil-bound Pu followed a similar pattern for all the original species, suggesting that the next step of Pu interaction mechanism with soil was rather independent of the original species. For both the Pu(V,VI) and Pu-organic species, the rainwater-desorption extract gave consistently higher KD values than that calculated from the rainwater-sorption data; whereas for Pu(III,IV), desorption KD values were more similar to sorption KD values. This supports the suggestion that the observed difference in Pu adsorption to soils reflects Pu-speciation in the water soluble phase, and that actual soil-Pu interactions are rather independent of the original speciation. Modelling of the extraction data show a different in association rate for the different Pu species, where the Pu(III,IV) has the fastest association rate as expected.

摘要

为评估放射性核素释放到环境中的长期后果,需要有关源项、迁移和转化过程、与土壤的相互作用(分配系数KD)以及生物摄取(浓缩系数CF)的信息。在核活动释放到环境中的人工放射性核素中,超铀元素是主要关注点,因为其半衰期极长,会在骨骼中积累且具有高放射性毒性。钚的产量比其他超铀元素更高,然而,其复杂的环境行为使环境评估变得复杂。钚的物理化学形态将决定其与土壤的相互作用,进而决定土壤作为污染物汇或潜在扩散源的程度。在本研究中,进行了动态示踪实验,向“玛雅克土壤 - 雨水系统”中添加不同的钚物种以获取分配系数KD值的信息。在规定的接触时间后,对样品进行顺序萃取,并将结果用于动态箱式模型以估计相互作用和固定速率。所有钚物种与土壤的相互作用似乎都很快,且遵循两步反应。在接触几周的时间内,Pu(III,IV)的分配系数KD(730±240 l/kg)比Pu(V,VI)(90±20 l/kg)和Pu(III,IV)-有机态(40 - 60 l/kg)大约高一个数量级。接触3个月后,仅两种有机结合的钚物种的分配系数KD显著降低。这表明与土壤的初始结合取决于雨水中的钚物种。仅接触1小时后,33%至40%的钚就强烈结合到土壤成分上,即仅能用浓硝酸萃取。对于所有原始物种,土壤结合钚的萃取遵循相似模式,这表明钚与土壤相互作用机制的下一步相当独立于原始物种。对于Pu(V,VI)和钚 - 有机物种,雨水解吸萃取得到的分配系数KD值始终高于根据雨水吸附数据计算的值;而对于Pu(III,IV),解吸分配系数KD值与吸附分配系数KD值更相似。这支持了以下观点:观察到的钚在土壤上吸附的差异反映了水溶性相中钚的形态,并且实际的土壤 - 钚相互作用相当独立于原始形态。萃取数据的建模显示不同钚物种的结合速率不同,其中Pu(III,IV)的结合速率如预期的那样最快。

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