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Contribution to the study of the desorption of fission gases formed in irradiated uranium oxide; Contribution a l'etude de la desorption des gaz de fission formes dans l'oxyde d'uranium irradie

Abstract

The release of {sup 133}Xe from irradiated UO{sub 2} has been studied in the temperature range 1300 to 1900 deg C, using various monocrystalline or sintered samples. Up to 1600 deg C, this release is proportional to the square root of the time and thus occurs essentially by diffusion. The apparent diffusion constant D' decreases and the activation energy of the corresponding process increases as the integrated neutron flux received by the fuel increases. As the density of the sintered samples decreases however, the activation energy of the release also decreases, so that the difference between D' values for sintered samples of different densities decreases as the temperature rises. Finally, above 1600 deg C, the fission gas release phenomenon is governed by UO{sub 2} evaporation, and all the different types of oxide studied have similar behaviors, characterized by poor retention of these gases. (authors) [French] La desorption du xenon 133 forme dans le bioxyde d'uranium irradie a ete etudiee dans l'intervalle de 1300 a 1900 C, a l'aide de differents echantillons monocristallins ou frittes. Jusqu'a 1600 C, elle s'effectue proportionnellement a la racine carree du temps, donc essentiellement par diffusion. La pseudo-constante de desorption D' decroit et l'energie d'activation du  More>>
Authors:
Berry, J -L; Darras, R; Roger, B [1] 
  1. Commissariat a l'Energie Atomique, Centre d'Etudes Nucleaires de Saclay, 91 - Gif-sur-Yvette (France)
Publication Date:
Sep 01, 1966
Product Type:
Technical Report
Report Number:
CEA-R-3021
Resource Relation:
Other Information: 15 refs; PBD: Sep 1966
Subject:
22 GENERAL STUDIES OF NUCLEAR REACTORS; DESORPTION; FISSION PRODUCT RELEASE; GASEOUS DIFFUSION; NEUTRON FLUX; TEMPERATURE DEPENDENCE; TEMPERATURE RANGE 1000-4000 K; URANIUM DIOXIDE; XENON 133
OSTI ID:
20468567
Research Organizations:
Commissariat a l'Energie Atomique, Centre d'Etudes Nucleaires de Saclay, 91 - Gif-sur-Yvette (France)
Country of Origin:
France
Language:
French
Other Identifying Numbers:
TRN: FR04R3021044277
Availability:
Available from INIS in electronic form
Submitting Site:
FRN
Size:
[24] pages
Announcement Date:

Citation Formats

Berry, J -L, Darras, R, and Roger, B. Contribution to the study of the desorption of fission gases formed in irradiated uranium oxide; Contribution a l'etude de la desorption des gaz de fission formes dans l'oxyde d'uranium irradie. France: N. p., 1966. Web.
Berry, J -L, Darras, R, & Roger, B. Contribution to the study of the desorption of fission gases formed in irradiated uranium oxide; Contribution a l'etude de la desorption des gaz de fission formes dans l'oxyde d'uranium irradie. France.
Berry, J -L, Darras, R, and Roger, B. 1966. "Contribution to the study of the desorption of fission gases formed in irradiated uranium oxide; Contribution a l'etude de la desorption des gaz de fission formes dans l'oxyde d'uranium irradie." France.
@misc{etde_20468567,
title = {Contribution to the study of the desorption of fission gases formed in irradiated uranium oxide; Contribution a l'etude de la desorption des gaz de fission formes dans l'oxyde d'uranium irradie}
author = {Berry, J -L, Darras, R, and Roger, B}
abstractNote = {The release of {sup 133}Xe from irradiated UO{sub 2} has been studied in the temperature range 1300 to 1900 deg C, using various monocrystalline or sintered samples. Up to 1600 deg C, this release is proportional to the square root of the time and thus occurs essentially by diffusion. The apparent diffusion constant D' decreases and the activation energy of the corresponding process increases as the integrated neutron flux received by the fuel increases. As the density of the sintered samples decreases however, the activation energy of the release also decreases, so that the difference between D' values for sintered samples of different densities decreases as the temperature rises. Finally, above 1600 deg C, the fission gas release phenomenon is governed by UO{sub 2} evaporation, and all the different types of oxide studied have similar behaviors, characterized by poor retention of these gases. (authors) [French] La desorption du xenon 133 forme dans le bioxyde d'uranium irradie a ete etudiee dans l'intervalle de 1300 a 1900 C, a l'aide de differents echantillons monocristallins ou frittes. Jusqu'a 1600 C, elle s'effectue proportionnellement a la racine carree du temps, donc essentiellement par diffusion. La pseudo-constante de desorption D' decroit et l'energie d'activation du processus correspondant croit lorsque le flux de neutrons integre recu par le combustible augmente. Cependant, lorsque la densite des frittes diminue, l'energie d'activation de desorption diminue egalement, de sorte que l'ecart entre les valeurs de D' relatives a des frittes de densites differentes se restreint lorsque, la temperature s'eleve. Finalement, au-dessus de 1600 C, l'evaporation de l'UO{sub 2} regit le phenomene de liberation des gaz de fission, et toutes les qualites d'oxyde etudiees presentent alors des comportements voisins a cet egard, caracterises par une mediocre retention de ces gaz. (auteurs)}
place = {France}
year = {1966}
month = {Sep}
}