From Laboratory Experiments to a Geological Disposal Vault: Calculation of Used Nuclear Fuel Dissolution Rates

1997 ◽  
Vol 506 ◽  
Author(s):  
S. Sunder ◽  
D.W. Shoesmith ◽  
M. Kolar ◽  
D.M. Leneveu

ABSTRACTCalculation of used nuclear fuel dissolution rates in a geological disposal vault requires a knowledge of the redox conditions in the vault. For redox conditions less oxidizing than those causing UO2 oxidation to the U3O7 stage, a thermodynamically-based model is appropriate. For more oxidizing redox conditions a kinetic or an electrochemical model is needed to calculate these rates. The redox conditions in a disposal vault will be affected by the radiolysis of groundwater by the ionizing radiation associated with the fuel. Therefore, we have calculated the alpha-, beta- and gamma-dose rates in water in contact with the reference used fuel in the Canadian Nuclear Fuel Waste Management Program (CNFWMP) as a function of cooling time. Also, we have determined dissolution rates of UO2 fuel as a function of alpha and gamma dose rates from our electrochemical measurements. These room-temperature rates are used to calculate the dissolution rates of used fuel at 100°C, the highest temperature expected in a container in the CNFWMP, as a function of time since emplacement. It is shown that beta radiolysis of water will be the main cause of oxidation of used CANDU fuel in a failed container. The use of a kinetic or an electrochemical corrosion model, to calculate fuel dissolution rates, is required for a period of ∼ 1000 a following emplacement of copper containers in the geologic disposal vault envisaged in the CNFWMP. Beyond this time period a thermodynamically-based model adequately predicts the fuel dissolution rates. The results presented in this paper can be adopted to calculate used fuel dissolution rates for other used UO2 fuels in other waste management programs.

1994 ◽  
Vol 353 ◽  
Author(s):  
S. Sunder ◽  
D.W. Shoesmith ◽  
N.H. Miller

AbstractEffects of alpha radiolysis of water on the corrosion of nuclear fuel (UO2) have been investigated in solutions at pH = 9.5, i.e., a value close to that expected in groundwaters at the depth of the disposal vault proposed in the Canadian nuclear fuel waste management program, CNFWMP. The corrosion potentials of UO2 electrodes exposed to the products of alpha radiolysis of water were monitored as a function of alpha flux and exposure time in a specially designed thin-layer cell. The oxidative dissolution rates of UO2 are calculated from the steady-state values of the corrosion potential using an electrochemical model. A procedure to predict the dissolution rate of used nuclear fuel in groundwater as a function of fuel cooling time is described, and illustrated by calculating the dissolution rates for the reference used fuel in the CNFWMP (Bruce CANDU reactor fuel, burnup 685 GJ/kg U). It is shown that the oxidative dissolution of used fuel in the CNFWMP will be important only for time periods ≤ 600 a at this burnup and assuming no decrease in pH.


2011 ◽  
Vol 46 (6) ◽  
pp. S301-S307 ◽  
Author(s):  
M.D. Wood ◽  
D. Copplestone

2006 ◽  
Vol 121 (3) ◽  
pp. 297-302 ◽  
Author(s):  
S. Dragović ◽  
Lj. Janković ◽  
A. Onjia

2019 ◽  
Vol 14 (30) ◽  
pp. 90-97
Author(s):  
Asia H. Al-Mashhadani

The gamma dose rates and specific activity of 137Cs, 60Co and 40K insamples of soil taken from places near the landfill radiation at Al-Tuwaitha site were measured using a portable NaI(Tl) detector. Theresults of gamma dose rates in samples were ranged from 52.6nGy.h-1 to 131nGy.h-1. Then the specific activity of 137Cs, 60Co and40K in soil were determined using high pure germanium (HPGe)detector. The specific activities were varied from 1.9 to 115500 Bq.kg-1 for 137Cs, from 6.37 to 616.5 Bq. kg-1 for 60Co, and from 3 to839.5 Bq. kg-1 for 40K. The corresponding health risk for the annualeffective dose equivalent varied from 1.85×10-14 to 15.7mSv/y. Theresults were compared with various international recommendations.


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