Uranyl peroxide enhanced nuclear fuel corrosion in seawater

被引:127
作者
Armstrong, Christopher R. [1 ]
Nyman, May [2 ]
Shvareva, Tatiana [1 ]
Sigmon, Ginger E.
Burns, Peter C. [3 ]
Navrotsky, Alexandra [1 ]
机构
[1] Univ Calif Davis, Agr & Technol Organized Res Unit, Peter A Rock Thermochem Lab & Nanomat Environm, Davis, CA 95616 USA
[2] Sandia Natl Labs, Albuquerque, NM 87185 USA
[3] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
关键词
calorimetry; actinyl peroxide; actinide; uranium; spent fuel; URANIUM-COMPOUNDS; UO2; STUDTITE; CALORIMETRY; DISSOLUTION; DIRECTIONS; PROGRESS; CRYSTAL; ALPHA;
D O I
10.1073/pnas.1119758109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Fukushima-Daiichi nuclear accident brought together compromised irradiated fuel and large amounts of seawater in a high radiation field. Based on newly acquired thermochemical data for a series of uranyl peroxide compounds containing charge-balancing alkali cations, here we show that nanoscale cage clusters containing as many as 60 uranyl ions, bonded through peroxide and hydroxide bridges, are likely to form in solution or as precipitates under such conditions. These species will enhance the corrosion of the damaged fuel and, being thermodynamically stable and kinetically persistent in the absence of peroxide, they can potentially transport uranium over long distances.
引用
收藏
页码:1874 / 1877
页数:4
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