Dissolution of high burn-up spent nuclear fuel at high-pH

被引:2
|
作者
Iglesias, Luis [3 ]
Kokinda, Jakub [3 ]
Serrano-Purroy, Daniel [4 ]
Martinez-Torrents, Albert [3 ]
Casas, Ignasi [5 ]
de Pablo, Joan [3 ,5 ]
Clarens, Frederic [3 ]
Gimenez, Javier [1 ,2 ,5 ]
机构
[1] Univ Politecn Cataluna, Dept Engn Quim, EEB, Eduard Maristany 10-14, Barcelona 08019, Catalonia, Spain
[2] Univ Politecn Cataluna, Barcelona Res Ctr Multiscale Sci & Engn, Eduard Maristany 10-14, Barcelona 08019, Catalonia, Spain
[3] Eurecat, Ctr Tecnol Gic Catalunya, Placa Ciencia 2, Manresa 08243, Spain
[4] European Commiss, Joint Res Ctr JRC, Karlsruhe, Germany
[5] Univ Politecn Cataluna, Dept Chem Engn, Barcelona Tech, Eduard Maristany 14, Barcelona 08019, Spain
基金
欧盟地平线“2020”;
关键词
spent nuclear fuel; high burnup fuel; cementitious waters; uranium; actinides; caesium; CORROSION PRODUCT DEPOSITS; OXIDATIVE DISSOLUTION; HYDROGEN-PEROXIDE; FISSION-PRODUCTS; INSTANT RELEASE; URANIUM; UO2; U(VI); SILICATE; SIMFUEL;
D O I
10.1515/ract-2023-0178
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The release of radionuclides from high-burnup spent nuclear fuel (SNF) segments was studied at pH = 13.2 as well as the effect of the presence of calcium and silicon. The aim was to ascertain the dissolution of SNF in solutions corresponding to a high-level nuclear waste repository including concrete in different structural parts. The release of uranium at pH = 13.2 was higher than at pH = 8.4 in bicarbonate medium, while the presence of calcium resulted in a decrease of the uranium concentrations in solutions, assumed to be the consequence of the formation of a secondary solid phase such as Ca2U2O7. Caesium release was found higher at pH = 13.2 as well, but it was not influenced by the presence of Ca and Si at long term. On the other hand, actinide elements (plutonium, neptunium and americium) dissolution decreased at pH = 13.2, probably because of the formation of secondary solid phases. On the contrary, ruthenium and technetium release at pH = 13.2 was found to be much higher than the measured at lower pH, perhaps due to the higher dissolution kinetics of the metallic inclusions at such pH.
引用
收藏
页码:817 / 828
页数:12
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