Sorption of environmentally relevant radionuclides (U(VI), Np(V)) and lanthanides (Nd(III)) on feldspar and mica
A safe storage of radioactive waste in repositories is an important task to protect humans and the environment from radio- and chemotoxicity. Long-term safety assessments predict the behavior of potential environmental contaminants like the actinides plutonium, uranium, or neptunium, in the near and...
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| Format: | Doctoral Thesis |
| Language: | English |
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Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden
2016
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| Online Access: | http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-197781 http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-197781 http://www.qucosa.de/fileadmin/data/qucosa/documents/19778/DissertationCRpdfA.pdf |
| Summary: | A safe storage of radioactive waste in repositories is an important task to protect humans and the environment from radio- and chemotoxicity. Long-term safety assessments predict the behavior of potential environmental contaminants like the actinides plutonium, uranium, or neptunium, in the near and far field of repositories. For such safety assessments, it is necessary to know the migration behavior of the contaminants in the environment, which is mainly dependent on the aquatic speciation, the solubility product of relevant solid phases, and the retardation due to sorption on surrounding minerals. Thus, an investigation of sorption processes of contaminants onto different minerals as well as the derivation of mineral specific surface complexation model (SCM) parameters is of great importance.
Feldspar and mica are widely distributed in nature. They occur as components of granite, which is considered as a potential host rock for a repository in Germany, and in numerous other rocks, and thus also in the far field of nearly all repositories. However, their sorption behavior with actinides has only been scarcely investigated until now. In order to better characterize these systems and subsequently to integrate these minerals into the long-term safety assessments, this work focuses on the investigation of the sorption behavior of U(VI), Np(V), and Nd(III) as analogue for An(III) onto the minerals orthoclase and muscovite, representing feldspars and mica, respectively. All investigations were performed under conditions relevant to the far field of a repository.
In addition to the extensive characterization of the minerals, batch sorption experiments, spectroscopic investigations, and surface complexation modeling were performed to elucidate the uptake and speciation of actinides on the mineral surfaces. In addition, the influence of microorganisms naturally occurring on the mineral surfaces and the effect of Ca2+ on U(VI) uptake on the minerals was studied. The obtained sorption curves exhibit a similar characteristic for orthoclase and muscovite. As expected Nd(III) shows the highest amount of sorption followed by U(VI) and finally Np(V). With spectroscopic investigations of the aquatic U(VI) solution in presence of Ca2+, the Ca2UO2(CO3)3 complex could be identified. Furthermore, with spectroscopic methods the U(VI) surface species onto orthoclase could be characterized, of which a novel uranium-carbonate surface species was observed.
Based on the results of batch experiments and spectroscopic methods new SCM parameters for the sorption of U(VI), Np(V), and Nd(III) onto orthoclase and for Np(V) and Nd(III) onto muscovite could be derived. SCM parameters for U(VI) sorption onto muscovite confirmed earlier investigations. The obtained SCM parameters increase the amount of data available for sorption processes onto feldspar and mica. With this the relevance of feldspars for the sorption of actinides and lanthanides could be shown. Thus, this work contributes to a better understanding of interactions of actinides and lanthanides, in particular U(VI), Np(V), and Nd(III), with mineral phases ubiquitous in the environment. This in turn adds confidence to long-term safety assessments essential for the protection of humans and the environment from the hazards of radioactive waste.
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