Surface-Mediated Formation of Pu(IV) Nanoparticles at the Muscovite-Electrolyte Interface

被引:27
作者
Schmidt, Moritz [1 ]
Lee, Sang Soo [1 ]
Wilson, Richard E. [1 ]
Knope, Karah E. [1 ]
Bellucci, Francesco [1 ]
Eng, Peter J. [2 ]
Stubbs, Joanne E. [2 ]
Soderholm, L. [1 ]
Fenter, P. [1 ]
机构
[1] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
[2] Univ Chicago, Ctr Adv Radiat Sources, Chicago, IL 60637 USA
基金
美国国家科学基金会; 美国能源部;
关键词
X-RAY REFLECTIVITY; PLUTONIUM TRANSPORT; ACID; SOLUBILITY; WATER; IONS; HYDROLYSIS; ADSORPTION; SPECTRA;
D O I
10.1021/es4037258
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The formation of Pu(IV)-oxo-nanoparticles from Pu(III) solutions by a surface-enhanced redox/polymerization reaction at the muscovite (001) basal plane is reported, with a continuous increase in plutonium coverage observed in situ over several hours. The sorbed Pu extends >70 angstrom from the surface with a maximum concentration at 10.5 angstrom and a total coverage of >9 Pu atoms per unit cell area of muscovite (0.77 mu g Pu/cm(2)) (determined independently by in situ resonant anomalous X-ray reflectivity and by ex-situ alpha-spectrometry). The presence of discrete nanoparticles is confirmed by high resolution atomic force microscopy. We propose that the formation of these Pu(IV) nanoparticles from an otherwise stable Pu(III) solution can be explained by the combination of a highly concentrated interfacial Pu-ion species, the Pu(III) Pu(IV) redox equilibrium, and the strong proclivity of tetravalent Pu to hydrolyze and form polymeric species. These results are the first direct observation of such behavior of plutonium on a naturally occurring mineral, providing insights into understanding the environmental transport of plutonium and other contaminants capable of similar redox/polymerization reactions.
引用
收藏
页码:14178 / 14184
页数:7
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