Evidence of a Nonphotochemical Mechanism for the Solid-State Formation of Uranyl Peroxide

被引:15
|
作者
Kirkegaard, Marie C. [1 ,2 ]
Miskowiec, Andrew [1 ]
Ambrogio, Michael W. [1 ]
Anderson, Brian B. [1 ,2 ]
机构
[1] Oak Ridge Natl Lab, Nucl Secur & Isotope Technol Div, Oak Ridge, TN 37831 USA
[2] Univ Tennessee, Bredesen Ctr Interdisciplinary Res & Grad Educ, Knoxville, TN 37996 USA
关键词
RAMAN-SPECTROSCOPY; HYDROGEN-PEROXIDE; WATER RADIOLYSIS; NUCLEAR-FUEL; MCR-ALS; STUDTITE; COMPLEXES; CORROSION; UO2; METASTUDTITE;
D O I
10.1021/acs.inorgchem.8b00512
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We have demonstrated the solid-state formation of a uranyl peroxide (UP) species from hydrated uranyl fluoride via a uranyl hydroxide intermediate, the first observation of a UP species formed in a solid-state reaction. Water vapor pressure is shown to be a driving factor of both the loss of fluorine and the subsequent formation of peroxo units. We have ruled out a photochemical mechanism for formation of the UP species by demonstrating that the same reaction occurs in the dark. A radiolytic mechanism is unlikely because of the low radioactivity of the sample material, suggesting the existence of a novel UP formation mechanism.
引用
收藏
页码:5711 / 5715
页数:5
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