Determination of dissolution rates of spent fuel in carbonate solutions under different redox conditions with a flow-through experiment

2001 ◽  
Vol 297 (3) ◽  
pp. 231-243 ◽  
Author(s):  
S Röllin ◽  
K Spahiu ◽  
U.-B Eklund
1989 ◽  
Vol 176 ◽  
Author(s):  
C. N. Wilson ◽  
W. J. Gray

ABSTRACTGaining a better understanding of the potential release behavior of water-soluble radionuclides is the focus of new laboratory spent fuel dissolution studies being planned in support of the Yucca Mountain Project. Previous studies have suggested that maximum release rates for actinide nuclides, which account for most of the long-term radioactivity in spent fuel, should be solubility-limited and should not depend on the characteristics or durability of the spent fuel waste form. Maximum actinide concentrations should be sufficiently low to meet the NRC annual release limits. Potential release rates for soluble nuclides such as 99Tc, 135Cs, 14C and 129I, which account for about 1-2% of the activity in spent fuel at 1000 years, are less certain and may depend on processes such as oxidation of the fuel in the repository air environment.Dissolution rates for several soluble nuclides have been measured from spent fuel specimens using static and semi-static methods. However, such tests do not provide a direct measurement of fuel matrix dissolution rates that may ultimately control soluble-nuclide release rates. Flow-through tests are being developed as a potential supplemental method for determining the matrix component of soluble-nuclide dissolution. Advantages and disadvantages of both semi-static and flow-through methods are discussed. Tests with fuel specimens representing a range of potential fuel states that may occur in the repository, including oxidized fuel, are proposed. Preliminary results from flow-through tests with unirradiated UO2 suggesting that matrix dissolution rates are very sensitive to water composition are also presented.


2021 ◽  
Vol 655 (1) ◽  
pp. 012024
Author(s):  
O.H. Ajesi ◽  
M.B. Latif ◽  
S.T. Gbenu ◽  
C. A. Onumejor ◽  
M. K. Fasasi ◽  
...  

2018 ◽  
Vol 480 ◽  
pp. 93-104 ◽  
Author(s):  
R. Kilgallon ◽  
S.M.V. Gilfillan ◽  
K. Edlmann ◽  
C.I. McDermott ◽  
M. Naylor ◽  
...  

1990 ◽  
Vol 231 ◽  
pp. 53-58 ◽  
Author(s):  
S. Alegret ◽  
J. Alonso ◽  
J. Bartroli ◽  
M. del Valle ◽  
N. Jaffrezic-Renault ◽  
...  
Keyword(s):  

1991 ◽  
Vol 113 (3) ◽  
pp. 206-210 ◽  
Author(s):  
D. Yogi Goswami

This paper analyzes velocity profiles for flow through circular tubes in laminar, turbulent, and transition region flows and how they affect measurement by flow-meters. Experimental measurements of velocity profiles across the cross-section of straight circular tubes were made using laser doppler velocimetry. In addition, flow visualization was done using the hydrogen bubble technique. Velocity profiles in the laminar and the turbulent flow are quite predictable which allow the determination of meter factors for accurate flow measurement. However, the profiles can not be predicted at all in the transition region. Therefore, for the accuracy of the flowmeter, it must be ensured that the flow is completely in the laminar regime or completely in the turbulent regime. In the laminar flow a bend, even at a large distance, affects the meter factor. The paper also discusses some strategies to restructure the flow to avoid the transition region.


2014 ◽  
Vol 78 (6) ◽  
pp. 1405-1416 ◽  
Author(s):  
U.-N. Berninger ◽  
G. Jordan ◽  
J. Schott ◽  
E. H. Oelkers

Natural hydromagnesite (Mg5(CO3)4(OH)2·4H2O) dissolution and precipitation experiments were performed in closed-system reactors as a function of temperature from 22.5 to 75ºC and at 8.6 < pH < 10.7. The equilibrium constants for the reaction Mg5(CO3)4(OH)2·4H2O + 6H+ = 5Mg2+ + 4HCO3– + 6H2O were determined by bracketing the final fluid compositions obtained from the dissolution and precipitation experiments. The resulting constants were found to be 1033.7±0.9, 1030.5±0.5 and 1026.5±0.5 at 22.5, 50 and 75ºC, respectively. Whereas dissolution rates were too fast to be determined from the experiments, precipitation rates were slower and quantified. The resulting BET surface areanormalized hydromagnesite precipitation rates increase by a factor of ~2 with pH decreasing from 10.7 to 8.6. Measured rates are approximately two orders of magnitude faster than corresponding forsterite dissolution rates, suggesting that the overall rates of the low-temperature carbonation of olivine are controlled by the relatively sluggish dissolution of the magnesium silicate mineral.


2011 ◽  
Vol 46 (5) ◽  
pp. 339-367 ◽  
Author(s):  
E. J. Llorent-Martínez ◽  
P. Ortega-Barrales ◽  
M. L. Fernández-De Córdova ◽  
A. Ruiz-Medina
Keyword(s):  

2012 ◽  
Vol 10 (3) ◽  
pp. 117-128 ◽  
Author(s):  
Ryan J. Bell ◽  
William B. Savidge ◽  
Strawn K. Toler ◽  
Robert H. Byrne ◽  
R. Timothy Short

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