Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-20T00:39:02.649Z Has data issue: false hasContentIssue false
  • English
  • Français

Thorium and Uranium Phosphate Syntheses and Lixiviation Tests for their Use as Hosts for Radwastes

Published online by Cambridge University Press:  15 February 2011

Michel Genet ,
N. Dacheux ,
C. Merigou  and
V. Brandel
Michel Genet
Affiliation:
Université de Paris-Sud, Institut de Physique Nucléaire/IN2P3, Groupe de Radiochimie, BP n°l, 91406 Orsay, Cedex, France.
N. Dacheux
Affiliation:
Université de Paris-Sud, Institut de Physique Nucléaire/IN2P3, Groupe de Radiochimie, BP n°l, 91406 Orsay, Cedex, France.
C. Merigou
Affiliation:
Université de Paris-Sud, Institut de Physique Nucléaire/IN2P3, Groupe de Radiochimie, BP n°l, 91406 Orsay, Cedex, France.
V. Brandel
Affiliation:
Université de Paris-Sud, Institut de Physique Nucléaire/IN2P3, Groupe de Radiochimie, BP n°l, 91406 Orsay, Cedex, France.
Get access

Abstract

Thorium and uranium phosphates were synthetized via soft chemistry and then calcined at high temperature, respectively up to 850 and 1170°C. Th3(PO4)4 was produced in agreement with published results.while the analog uranium phosphate : U3(PO4)4 was not found. Instead, we found we had made a new mixed valence compound : U(UO2)(PO4)2, for which crystal structure, absorption spectrum in ultraviolet and visible, and X-ray photoelectron spectroscopy were done. All of these experiments confirmed the presence of uranium in both tetravalent and hexavalent states.

Lixiviation of thorium phosphate labelled with radioactive isotopes : 227Th and 223Ra allowed us to determine the upper limit of the solubility for this compound = 7.6xl0–11 M and, the percentage of 223Ra released in deionized water (about 5xl0–3%).

Similar lixiviation tests on U(UO2)(PO4)2 labelled with 230U (radiochemically produced) gave an uranium solubility value 10 times greater than uranium measured by laser spectrofluorimetry. This discrepancy is attributed to the radiation chemistry inherent in the use of radioactive isotope at high specific activity. The lixiviated uranium fraction from U(UO2)(PO4)2 is seven to eight orders of magnitude higher than for thorium. Unexpected behaviour was observed for uranium solubility which increases by two orders of magnitude after 2000 hours of lixiviation. This phenomenon is not yet understood.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 353: Symposium – Scientific Basis for Nuclear Waste Management XVIII , 1994 , 799
Copyright
Copyright © Materials Research Society 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1] Boatner, L.A. and Sales, B. C., in Radioactive waste forms for the future, edited by Lutze, W. and Ewing, R.C. (Elsevier Science Publishers B.V., 1988), p. 495.Google Scholar
[2] Shankar, J. and Khubchandani, P.G.; Anal. Chem.; 29 (9), 1375 (1957).Google Scholar
[3] Burdese, A and Borlera, M.L.; Ann. Chim. Roma; 53, 344 (1963).Google Scholar
[4] Laud, K.R. and Hummel, F.A.; J. Amer. Chem. Soc.; 57, 296 (1971).Google Scholar
[5] Baglan, N., Thesis, Paris-Sud University, Orsay, 1992.Google Scholar
[6] Baglan, N., Fourest, B., Guillaumont, R., Blain, G., Le Du, J.F., and Genet, M.; New J. Chemistry;18, 809 (1994).Google Scholar
[7] Dunn, H. W., Report n° 2092, (Oak Ridge National Laboratory, Oak Ridge, TN), 1956.Google Scholar
[8] Schaekers, J.M.; J. of Thermal Analysis; 6, 145 (1974).Google Scholar
[9] Bamberger, C.E., Haire, R.G., Begun, G.M. and Hellwege, H.E.; J. of the Less Common Metals; 102, 179 (1984).Google Scholar
[10] Dacheux, N., Brandel, V. and Genet, M.; New. J. Chem.; (under press).Google Scholar
[11] Bénard, P. Louër, JD, Dacheux, N.,Brandel, V. and Genet, M.; Chem. Mat.; 6, 1049, (1994).Google Scholar
[12] Hubert, S., Chong, L.S., Genet, M. and Auzel, F.; J. Solid State Chem.; 61, 252 (1986).Google Scholar
[13] Moulin, C., Beaucaire, C., Decambox, P. and Mauchien, P.; Anal. Chim. Acta; 238, 291, (1990).Google Scholar