Behaviour of Mo(VI), Eu(III) and U(VI) in calcium-silicate-hydrate phases: Immobilisation and dynamic remobilisation under repository-relevant conditions

Calcium-silicate-hydrate (C-S-H) phases play an essential role as a geotechnical barrier in high-level nuclear waste (HLW) repositories. To guarantee the long-term safety of a HLW disposal site, it is important to know how and to which degree radionuclides are retained by C-S-H phases. To this date, only little to no data on the remobilisation dynamics of the repository-relevant elements Mo(VI), Eu(III) and U(VI) under realistic conditions are available. In this study, C-S-H phases incorporating these elements were synthesised, the element immobilisation was quantified via ICP-QQQ and their structure was investigated via X-ray diffractometry. All C-S-H phases had a calcium-silicon ratio (C/S) of 1.066 ± 0.003 and no relevant structural influences of the studied elements could be observed. In all cases, quantitative immobilization was observed for Eu(III) and U(VI), whereas Mo(VI) was retained/incorporated to only about 50%. Afterwards, their leaching behaviour with ultrapure water was studied in batch and mini-column experiments (MCE). Mo(VI) was remobilised quickly, while Eu(III) and U(VI) were retained nearly quantitatively. Due to the more realistic and therefore more representative conditions, further experiments to investigate the effects of three repository-relevant parameters were conducted only using MCE. A higher ionic strength significantly enhanced U(VI) remobilisation, while Eu(III) and Mo(VI) remained nearly unaffected. The displacement agents Fe(III) and Tb(III) only affected Mo(VI)’s remobilisation by retarding it. The addition of a complexing agent (2-phosphonobutane-1,2,4-tricarboxylic acid; PBTC) led to a delayed remobilisation of Mo(VI), while Eu(III) and U(VI) were remobilised to some degree after sufficient PBTC eluation. Overall, this work delivers important information on key processes relevant to nuclear waste disposal. • Successful incorporation of Mo(VI), Eu(III) and U(VI) into C-S-H • High ionic strength can influence Ca(II), Si(VI) and U(VI) remobilisation from C-S-H • Fe(III) and Tb(III) influences Ca(II), Si(VI) and Mo(VI) remobilisation from C-S-H • PBTC influences Ca(II), Si(VI), Mo(VI), Eu(III) and U(VI) remobilisation from C-S-H • Column experiments (MCE) provide better understanding in remobilisation dynamics

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Journal
Applied Geochemistry
Published
2026-01-06
DOI
https://doi.org/10.1016/j.apgeochem.2026.106684
Primary Topic
Radioactive element chemistry and processing
Type
article
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article

Behaviour of Mo(VI), Eu(III) and U(VI) in calcium-silicate-hydrate phases: Immobilisation and dynamic remobilisation under repository-relevant conditions

Ralf Kautenburger, Aaron Haben, Nico Bachmann, Jan Jakob Langer
Applied Geochemistry
Radioactive element chemistry and processing
article

Behaviour of Mo(VI), Eu(III) and U(VI) in calcium-silicate-hydrate phases: Immobilisation and dynamic remobilisation under repository-relevant conditions

Ralf Kautenburger, Aaron Haben, Nico Bachmann, Jan Jakob Langer
article en

Abstract

Calcium-silicate-hydrate (C-S-H) phases play an essential role as a geotechnical barrier in high-level nuclear waste (HLW) repositories. To guarantee the long-term safety of a HLW disposal site, it is important to know how and to which degree radionuclides are retained by C-S-H phases. To this date, only little to no data on the remobilisation dynamics of the repository-relevant elements Mo(VI), Eu(III) and U(VI) under realistic conditions are available. In this study, C-S-H phases incorporating these elements were synthesised, the element immobilisation was quantified via ICP-QQQ and their structure was investigated via X-ray diffractometry. All C-S-H phases had a calcium-silicon ratio (C/S) of 1.066 ± 0.003 and no relevant structural influences of the studied elements could be observed. In all cases, quantitative immobilization was observed for Eu(III) and U(VI), whereas Mo(VI) was retained/incorporated to only about 50%. Afterwards, their leaching behaviour with ultrapure water was studied in batch and mini-column experiments (MCE). Mo(VI) was remobilised quickly, while Eu(III) and U(VI) were retained nearly quantitatively. Due to the more realistic and therefore more representative conditions, further experiments to investigate the effects of three repository-relevant parameters were conducted only using MCE. A higher ionic strength significantly enhanced U(VI) remobilisation, while Eu(III) and Mo(VI) remained nearly unaffected. The displacement agents Fe(III) and Tb(III) only affected Mo(VI)’s remobilisation by retarding it. The addition of a complexing agent (2-phosphonobutane-1,2,4-tricarboxylic acid; PBTC) led to a delayed remobilisation of Mo(VI), while Eu(III) and U(VI) were remobilised to some degree after sufficient PBTC eluation. Overall, this work delivers important information on key processes relevant to nuclear waste disposal. • Successful incorporation of Mo(VI), Eu(III) and U(VI) into C-S-H • High ionic strength can influence Ca(II), Si(VI) and U(VI) remobilisation from C-S-H • Fe(III) and Tb(III) influences Ca(II), Si(VI) and Mo(VI) remobilisation from C-S-H • PBTC influences Ca(II), Si(VI), Mo(VI), Eu(III) and U(VI) remobilisation from C-S-H • Column experiments (MCE) provide better understanding in remobilisation dynamics

Applied GeochemistryVol. 198
Saarland University (DE)
Clean water and sanitation
Openalex Percentile: Top 95%
Radioactive element chemistry and processing
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