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Diffuse reflectance spectroscopy of Pu ions in zirconolite and perovskite

Published online by Cambridge University Press:  17 March 2011

E. R. Vance ,
K. S. Finnie ,
Y. Zhang  and
B. D. Begg
E. R. Vance
Affiliation:
Materials and Engineering Science, ANSTO, Menai, NSW 2234, Australia, erv@ansto.gov.au
K. S. Finnie
Affiliation:
Materials and Engineering Science, ANSTO, Menai, NSW 2234, Australia, erv@ansto.gov.au
Y. Zhang
Affiliation:
Materials and Engineering Science, ANSTO, Menai, NSW 2234, Australia, erv@ansto.gov.au
B. D. Begg
Affiliation:
Materials and Engineering Science, ANSTO, Menai, NSW 2234, Australia, erv@ansto.gov.au
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Abstract

Diffuse reflectance spectroscopy measurements at ambient temperatures have been made over the near infrared-visible range (5000-25000 cm−1) on polycrystalline ceramic zirconolite (CaZrTi2O7) and perovskite (CaTiO3) samples doped with Pu4+. The Pu concentrations were varied between 0.001 and 0.1 formula units. The Pu ions gave rise to a number of unresolved intraconfigurational f-f electronic absorption bands of a few hundred cm−1 bandwidth. Pu ions were targeted to substitute in the Ca sites as either trivalent or tetravalent species and as tetravalent species in the Zr site of zirconolite by the appropriate choice of charge compensation and firing atmosphere. There was approximate agreement of the Kubelka-Munk absorption intensities with Beer's Law for the different Pu4+ substitution schemes, apart from some “new” bands, attributed to impurities, observed in the most dilute zirconolite sample. No clear spectral differences were evident when Pu4+ was targeted to Ca or Zr sites in zirconolite. Samples prepared in reducing atmospheres with a view to producing Pu3+ were strongly absorbing, leading to suppression of Pu transitions.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 824: Symposium CC – Scientific Basis for Nuclear Waste Management XXVIII , 2004 , CC4.10
Copyright
Copyright © Materials Research Society 2004

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References

[1] Ebbinghaus, B. B., VanKonynenburg, R. A., Ryerson, F. J., Vance, E. R., Stewart, M. W. A., Jostsons, A., Allender, J. S., Rankin, T. and Congdon, J., Waste Management '98 (CD-ROM; sess65/65-04), WM Symposia Inc., Tucson, AZ, 1998.Google Scholar
[2] Vance, E. R., Jostsons, A., Moricca, S., Stewart, M. W. A., Day, R. A., Begg, B. D., Hambley, M. J., Hart, K. P. and Ebbinghaus, B. B., in Environmental Issues and Waste Management Technologies in the Ceramic and Nuclear Industries IV, ed. Marra, J. C. and Chandler, G. T., ACS Ceramic Transactions Vol. 93, Columbus, OH, USA, 323–9 (1999).Google Scholar
[3] Begg, B. D., Vance, E. R. and Conradson, S. D., J. Alloys and Compounds 271–273 221–6 (1998).Google Scholar
[4] Begg, B. D., Vance, E. R., Hunter, B. A. and Hanna, J. V., J. Mater. Res., 13, 3181–90 (1997).Google Scholar
[5] Sliva, R. J. and Nitsche, H., in Advances in Plutonium Chemistry 1967-2000, Ed. Hoffman, D. C., American Nuclear Society, La Grange Park, IL, USA, pp.89–117 (2002).Google Scholar
[6] Vance, E. R., Lumpkin, G. R., Carter, M. L., Cassidy, D. J., Ball, C. J., Day, R. A. and Begg, B. D., J. Amer. Ceram. Soc., 85, 1853–9 (2002).Google Scholar