The Release of Uranium, Plutonium, Cesium, Strontium, Technetium and Iodine from Spent Fuel under Unsaturated Conditions

1996 ◽  
Vol 74 (s1) ◽  
Author(s):  
P. A. Finn ◽  
J. C. Hoh ◽  
S. F. Wolf ◽  
S. A. Slater ◽  
J. K. Bates
Keyword(s):  
1999 ◽  
Vol 556 ◽  
Author(s):  
V. M. Oversby

AbstractIn the early 1980s, tests of the leaching behavior of spent light water reactor fuel were conducted in Sweden by SKB and in the USA by the NNWSI Project. Both organizations used fuels with similar burnup, leaching solutions with similar chemical compositions, and conducted the tests at ambient hot cell temperature. Most of the test results were closely similar. The exception was in the recovery of actinide elements at the end of leaching cycles. In the NNWSI tests, the test vessels were stripped with nitric acid at the end of the leaching cycle. When the actinide inventories recovered in the original leaching cycle plus vessel rinse solutions were added to the amount recovered from the acid stripping, the relative abundances of uranium, plutonium, and other actinides were approximately the same as their inventories in the fuel samples. In the SKB tests, the materials recovered from stripping the leaching vessels were low in amount and interpreted to be fine fuel fragments. Only a few percent of the plutonium inventory that would correspond to the uranium recovered in solution was accounted for in the solution samples. To investigate the reasons for this difference in recovery of the actinides, a new test was undertaken using a fuel sample that had been leached for several years using the SKB methods. The fuel was removed from the cladding after a total of a bit more than two years of leaching inside the cladding. The bare fuel was then leached for several cycles using a geometry that simulated the NNWSI tests and a test procedure that was similar to that used in the NNWSI tests. The cladding from which the fuel was removed was also leached in a separate vessel in parallel with the bare fuel leaching. This paper presents the results of the test series and discusses the effects of specimen geometry on the mobility of actinides during leaching. During leaching of spent fuel inside the original cladding, a secondary phase containing Pu seems to form. This phase appears to be less easily dissolved than spent fuel itself.


Author(s):  
Aleksander S. Gerasimov ◽  
Boris R. Bergelson ◽  
Tamara S. Zaritskaya ◽  
Georgy V. Tikhomirov

Accumulation and subsequent storage of actinides from uranium, plutonium, and thorium spent fuel of PWR type reactor is discussed in the paper. During period of accumulation 100 or 300 years, actinides are periodically introduced in the storage facility. Subsequent period of 300 000 years is long-term storage without introduction of new portions of spent fuel. This time includes both period of controllable storage and ultimate geological storage. Decay heat power of actinides was calculated. It affects heat removal system of the storage facility. Maximal decay heat power of actinides from plutonium spent fuel corresponding to the end of the period of accumulation of 100 years is 2.5 times higher than that of uranium spent fuel. Maximal decay heat power of actinides from uranium spent fuel is 1.2 times higher than that of thorium spent fuel.


Equipment ◽  
2006 ◽  
Author(s):  
D. Sujish ◽  
C. Meikandamurthy ◽  
T. R. Ellappan ◽  
M. Rajan ◽  
G. Vaidyanathan

1982 ◽  
Author(s):  
E. DRAPER ◽  
GEORGE COULBOURN
Keyword(s):  

2020 ◽  
Vol 86 (12) ◽  
pp. 15-22
Author(s):  
N. A. Bulayev ◽  
E. V. Chukhlantseva ◽  
O. V. Starovoytova ◽  
A. A. Tarasenko

The content of uranium and plutonium is the main characteristic of mixed uranium-plutonium oxide fuel, which is strictly controlled and has a very narrow range of the permissible values. We focused on developing a technique for measuring mass fractions of uranium and plutonium by controlled potential coulometry using a coulometric unit UPK-19 in set with a R-40Kh potentiostat-galvanostat. Under conditions of sealed enclosures, a special design of the support stand which minimized the effect of fluctuations in ambient conditions on the signal stability was developed. Optimal conditions for coulometric determination of plutonium and uranium mass fractions were specified. The sulfuric acid solution with a molar concentration of 0.5 mol/dm3 was used as a medium. Lead ions were introduced into the background electrolyte to decrease the minimum voltage of hydrogen reduction to –190 mV. The addition of aluminum nitride reduced the effect of fluoride ions participating as a catalyst in dissolving MOX fuel samples, and the interfering effect of nitrite ions was eliminated by introducing a sulfamic acid solution into the cell. The total content of uranium and plutonium was determined by evaluation of the amount of electricity consumed at the stage of uranium and plutonium co-oxidation. Plutonium content was measured at the potentials, at which uranium remains in the stable state, which makes it possible to subtract the contribution of plutonium oxidation current from the total oxidation current. The error characteristics of the developed measurement technique were evaluated using the standard sample method and the real MOX fuel pellets. The error limits match the requirements set out in the specifications for MOX fuel. The technique for measuring mass fractions of uranium and plutonium in uranium-plutonium oxide nuclear fuel was certified. The relative measurement error of the mass fraction of plutonium and uranium was ±0.0070 and ±0.0095, respectively. The relative error of the ratio of the plutonium mass fraction to the sum of mass fractions of uranium and plutonium was ±0.0085.


Kerntechnik ◽  
2020 ◽  
Vol 85 (1) ◽  
pp. 38-53
Author(s):  
M. J. Leotlela ◽  
I. Petr ◽  
A. Mathye

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