J Rothe et al 2009 J. Phys.: Conf. Ser. 190 012188 doi:10.1088/1742-6596/190/1/012188
J Rothe, C Walther, B Brendebach, S Büchner, M Fuss, M A Denecke and H Geckeis
Show affiliationsThe long term radiotoxicity of spent nuclear fuel disposed of in deep underground repositories after discharge from nuclear power reactors is determined by actinide elements, mainly plutonium. Water intrusion into the repository might cause container corrosion and leaching of the waste matrices, leading to the release of Pu and other actinides into the geological environment. Performance assessment for a future nuclear waste repository requires detailed knowledge on actinide aqueous chemistry in the aquifer surrounding the disposal site. Tetravalent actinides exhibit a strong tendency towards hydrolysis and subsequent polymerization and/or colloid formation. These species provide a potential pathway for migration of actinides away from the repository. Therefore, it is of fundamental interest to study their generation and properties in-situ. To this end, X-ray Absorption Fine Structure Spectroscopy (XAFS) at the INE-Beamline for actinide research at ANKA, Electrospray Mass-Spectrometry (ESI TOF-MS) and Laser Induced Breakdown Detection (LIBD) are combined at FZK-INE in a comprehensive attempt to characterize Zr(IV) (An(IV) analogue), Th(IV) and Pu(IV) polymerization and colloid formation.
28.41.Kw Radioactive wastes, waste disposal
Soft matter, liquids and polymers
Condensed matter: electrical, magnetic and optical
Issue 1 (2009)
J Rothe et al 2009 J. Phys.: Conf. Ser. 190 012188
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