globalchange  > 过去全球变化的重建
DOI: 10.2172/1240745
报告号: DOE-TXAM--06820
报告题名:
Plutonium Immobilization and Mobilization by Soil Organic Matter
作者: Santschi, Peter H.; Schwehr, Kathleen A.; Xu, Chen; Athon, Matthew; Ho, Yi-Fang; Hatcher, Patrick G.; Didonato, Nicole; Kaplan, Daniel I.
出版年: 2016
发表日期: 2016-03-08
总页数: 2
国家: 美国
语种: 英语
英文关键词: Plutonium ; Speciation ; Natural Organic Matter Carrier Phases ; Hydroxamates
中文主题词: ; ; 有机物 ; 沉积物 ; 有机碳 ; PH ; 地表水 ; PH值
主题词: CARBON ; NITROGEN ; ORGANIC MATTER ; SEDIMENTS ; ORGANIC CARBON ; PH ; SURFACE WATER
英文摘要: The human and environmental risks associated with Pu disposal, remediation, and nuclear accidents scenarios stems mainly from the very long half-lives of several of its isotopes. The SRS, holding one-third of the nation’s Pu inventory, has a long-term stewardship commitment to investigation of Pu behavior in the groundwater and downgradient vast wetlands. Pu is believed to be essentially immobile due to its low solubility and high particle reactivity to mineral phase or natural organic matter (NOM). For example, in sediments collected from a region of SRS, close to a wetland and a groundwater plume, 239,240Pu concentrations suggest immobilization by NOM compounds, as Pu correlate with NOM contents. Micro-SXRF data indicate, however, that Pu does not correlate with Fe. However, previous studies reported Pu can be transported several kilometers in surface water systems, in the form of a colloidal organic matter carrier, through wind/water interactions. The role of NOM in both immobilizing or re-mobilizing Pu thus has been demonstrated. Our results indicate that more Pu (IV) than (V) was bound to soil colloidal organic matter (COM), amended at far-field concentrations. Contrary to expectations, the presence of NOM in the F-Area soil did not enhance Pu fixation to the organic-rich soil, when compared to the organic-poor soil or the mineral phase from the same soil source, due to the formation of COM-bound Pu. Most importantly, Pu uptake by organic-rich soil decreased with increasing pH because more NOM in the colloidal size desorbed from the particulate fraction at elevated pH, resulting in greater amounts of Pu associated with the COM fraction. This is in contrast to previous observations with low-NOM sediments or minerals, which showed increased Pu uptake with increasing pH levels. This demonstrates that despite Pu immobilization by NOM, COM can convert Pu into a more mobile form. Sediment Pu concentrations in the SRS F-Area wetland were correlated to total organic carbon and total nitrogen contents and even more strongly to hydroxamate siderophore (HS) concentrations. The HS were detected in the particulate or colloidal phases of the sediments but not in the low molecular fractions (< 1000 Da). Macromolecules which scavenged the majority of the potentially mobile Pu were further separated from the bulk mobile organic matter fraction (“water extract”) via isoelectric focusing experiment (IEF). An ESI FTICR-MS spectral comparison of the IEF extract and a siderophore standard (desferrioxamine; DFO) suggested the presence of HS functionalities in the IEF extract.
URL: http://www.osti.gov/scitech/servlets/purl/1240745
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资源类型: 研究报告
标识符: http://119.78.100.158/handle/2HF3EXSE/42203
Appears in Collections:过去全球变化的重建
影响、适应和脆弱性
科学计划与规划
气候变化与战略
全球变化的国际研究计划
气候减缓与适应
气候变化事实与影响

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Recommended Citation:
Santschi, Peter H.,Schwehr, Kathleen A.,Xu, Chen,et al. Plutonium Immobilization and Mobilization by Soil Organic Matter. 2016-01-01.
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