Application de techniques de microanalyse pour la caractérisation de combustibles céramiques nucléaires irradiés
S. Brémier, P. Poeml, F. Laheurte and R. Hasnaoui
European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, DE-76125 Karlsruhe, Germany
Microbeam
analysis is widely used in the nuclear power industry. It is used
for routine post-irradiation examination and for research into the
mechanisms affecting safe operation of the nuclear fuel. The techniques
most commonly used are wave-length dispersive electron probe
microanalysis (WDS-EPMA), scanning electron microscopy (SEM) and
secondary ion mass spectrometry (SIMS). Other microbeam analysis
techniques that have been successfully applied to irradiated nuclear
fuel are transmission and replica electron microscopy (TEM and REM),
micro X-ray fluorescence (micro-XRF) and micro X-ray diffraction
(micro-XRD). SEM, TEM and REM have been mainly used to study the
evolution of fission gas bubbles, which cause the fuel to swell during
irradiation [1-3], and micro-XRD has been used to investigate the
change in lattice parameter caused by irradiation damage and the
build-up of fission products during irradiation and to assess their
influence on the transformation of the fuel microstructure after
prolonged irradiation [4].
WDS-EPMA is the microbeam analysis technique most widely available in
nuclear research centres around the world. From the perspective of
investigating irradiated nuclear fuel, this technique has a number of
limitations. The main drawback is that it does not measure
isotopes. A further shortcoming is the detection limit, which for
a radioactive sample is at best 200 ppm [5]. In addition, the
fission gas krypton cannot be measured because the second order M1 U
X-ray line coincides with the Kr L1 line and the Kr K X-ray lines have
a high critical excitation energy of 14.3 keV. Finally, owing to the
shallow electron penetration in nuclear fuel, the fission gas trapped
in pores and bubbles larger than about 0.1 m cannot be detected
[6,7]. These deficiencies have been overcome by combining EPMA
with micro-XRF [8] and SIMS [9].
This presentation will recall some background information about nuclear
fuel rods and their irradiation, followed by a description of the
features that set apart the microbeam analysis of irradiated nuclear
fuel from standard practice on "cold" materials. Finally, specific
examples illustrating the past and present use of microbeam analysis in
nuclear research are discussed, with emphasis on most valuable and
unique sets of results.
References
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[2] I.L.F. Ray, H. Thiele and Hj. Matzke, J. Nucl. Mater. 188 (1992) 90-95.
[3] M. Mogensen, C.T. Walker, I.L.F. Ray and M. Coquerelle, J. Nucl. Mater. 131 (1985) 162-171.
[4] J. Spino and D. Papaioanou, J. Nucl Mater. 281 (2000) 146-162.
[5] C.T. Walker, J. Anal. At. Spectrom. 14 (1999) 447-454.
[6] C. Ronchi and C.T. Walker, J. Phys. D: Appl. Phys. 13 (1980) 2175-2184
[7] M. Verwerft, J. Nucl. Mater. 282 (2000) 97-111.
[8] C.T. Walker and M. Mogensen, J. Nucl. Mater. 149 (1987) 121-131.
[9] C.T. Walker, S. Bremier, S. Portier, R. Hasnaoui, W. Goll, J. Nucl. Mater. 393 (2009) 212-223.
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