Modelling experimental results on radiolytic processes at the spent fuel water interface.: I.: Radiolysis products and U release

被引:5
作者
Bruno, J [1 ]
Cera, E [1 ]
Eriksen, TE [1 ]
Grivé, M [1 ]
Ripoll, S [1 ]
机构
[1] Enviros Spain SL, Valldoreix 08197, Spain
来源
SCIENTIFIC BASIS FOR NUCLEAR WASTE MANAGEMENT XXVII | 2004年 / 807卷
关键词
D O I
10.1557/PROC-807-397
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Experimental and modelling efforts in the last decade in the frame of nuclear waste management field have been focused on studying the role of the UO2 surfaces in poising the redox state of solid/water systems. For this purpose, an experimental programme was developed consisting on dissolution experiments with PWR spent fuel fragments in an anoxic environment and by using different solution compositions. The collected data so far, indicate that production and fate of radiolysis products follow the same trends independently on the solution composition used in the tests. Hydrogen and oxygen concentrations show an initial increase with time until reaching a constant concentration. The trend observed for hydrogen peroxide is a decrease at short contact times to reach again a constant concentration with time. These steady-states indicate an overall balance of the generated radiolytic species. Modelling work indicates that uranium dissolution is controlled by the oxidation of the spent fuel matrix in 10mM bicarbonate solutions while in the tests carried out at lower or without carbonate concentrations uranium in the aqueous phase is governed by the precipitation of schoepite. These results are determinant to highlight that reducing conditions are restored in the aqueous phase in relatively short periods of time and at short distances away from the dynamic redox spent fuel/ water interface.
引用
收藏
页码:397 / 402
页数:6
相关论文
共 10 条
[1]   Advanced oxidation processes (AOP) for water purification and recovery [J].
Andreozzi, R ;
Caprio, V ;
Insola, A ;
Marotta, R .
CATALYSIS TODAY, 1999, 53 (01) :51-59
[2]  
BRUNO J, 1999, TR9926 SKB
[3]  
CASAS I, 1994, TR9404 AECLSKB
[4]  
Cera E, 2002, 8 EC NAT AN WORK GRO, P183
[5]  
CHRISTENSEN H, 1990, NS9085
[6]   A CLASSIFICATION SCHEME FOR HOMOGENEOUS METAL-CATALYZED OXIDATIONS BY O-2 [J].
DRAGO, RS ;
BEER, RH .
INORGANICA CHIMICA ACTA, 1992, 198 :359-367
[7]  
EDWARDS JO, 1992, CATALYTIC OXIDATIONS, P111
[8]   Dissolution of irradiated fuel: A radiolytic mass balance study [J].
Eriksen, TE ;
Eklund, UB ;
Werme, L ;
Bruno, J .
JOURNAL OF NUCLEAR MATERIALS, 1995, 227 (1-2) :76-82
[9]  
NEEDES CRS, 1973, 7073 NAT I MET
[10]   Fuel corrosion processes under waste disposal conditions [J].
Shoesmith, DW .
JOURNAL OF NUCLEAR MATERIALS, 2000, 282 (01) :1-31