001     1016753
005     20240708133807.0
037 _ _ |a FZJ-2023-03739
100 1 _ |a Klinkenberg, Martina
|0 P:(DE-Juel1)130364
|b 0
|e Corresponding author
|u fzj
111 2 _ |a 21st Jena Remediation Symposium
|c Jena
|d 2023-10-04 - 2023-10-06
|w Germany
245 _ _ |a Solid-solution formation of (Ba,Sr,Ra)SO4: Microscopic approaches
260 _ _ |c 2023
336 7 _ |a Conference Paper
|0 33
|2 EndNote
336 7 _ |a INPROCEEDINGS
|2 BibTeX
336 7 _ |a conferenceObject
|2 DRIVER
336 7 _ |a CONFERENCE_POSTER
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336 7 _ |a Output Types/Conference Poster
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336 7 _ |a Poster
|b poster
|m poster
|0 PUB:(DE-HGF)24
|s 1696842055_25867
|2 PUB:(DE-HGF)
|x Invited
520 _ _ |a The minerals of the isostructural barite ((Ba,Sr)SO4) group are frequently occurring and characterized by their low solubility. These sulfates are associated with the formation of technically enhanced naturally occurring radioactive material (TENORM). The radioactivity of TENORM is often a result of solid solution formation with 226Ra because of the higher thermodynamic stability compared to the pure endmember RaSO4. The (Ra,Ba,Sr)SO4 is also relevant for the safety assessment of deep geological repositories for spent nuclear fuel. In this contribution, the application of microscopic approaches on the solid-solution formation of (Ba,Sr,Ra)SO4 to understand macroscopic observations will be discussed.A combination of scanning electron microscopy (SEM), energy dispersive x-ray spectrometry (EDX), focused ion beam (FIB), transmission electron microscopy (TEM) as well as time of flight secondary ion mass spectroscopy (ToF-SIMS) and atom probe tomography (APT) was applied to unravel the up-take of 226Ra into (Ba,Sr,Ra)SO4 on a molecular scale. SEM-EDX was used to follow the morphological and chemical evolution of the sulfate particles during the Ra-uptake. The Ra-uptake into the solid was observed by a 3D analysis of complete grains via ToF-SIMS. The FIB, producing very small samples and extremely thin samples for TEM and atom probe tomography (APT), enables the detailed investigation of even highly radioactive materials due to the low radioactivity of the FIB sections. TEM and APT were applied to unravel the details of this recrystallization process from the solid materials perspective, indicating an important role of fluid inclusions and internal porosity typical for these sulfates. Our studies not only show that 226Ra is taken up structurally during recrystallisation of (Ba,Sr)SO4, but also that kinetically controlled initial stages eventually are followed by thermodynamically controlled Ra-uptake which can be described via solid-solution aqueous-solution modeling.
536 _ _ |a 1411 - Nuclear Waste Disposal (POF4-141)
|0 G:(DE-HGF)POF4-1411
|c POF4-141
|f POF IV
|x 0
700 1 _ |a Brandt, Felix
|0 P:(DE-Juel1)144040
|b 1
|u fzj
700 1 _ |a Barthel, Juri
|0 P:(DE-Juel1)130525
|b 2
|u fzj
700 1 _ |a Bosbach, Dirk
|0 P:(DE-Juel1)130324
|b 3
|u fzj
909 C O |o oai:juser.fz-juelich.de:1016753
|p VDB
910 1 _ |a Forschungszentrum Jülich
|0 I:(DE-588b)5008462-8
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910 1 _ |a Forschungszentrum Jülich
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910 1 _ |a Forschungszentrum Jülich
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910 1 _ |a Forschungszentrum Jülich
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|6 P:(DE-Juel1)130324
913 1 _ |a DE-HGF
|b Forschungsbereich Energie
|l Nukleare Entsorgung, Sicherheit und Strahlenforschung (NUSAFE II)
|1 G:(DE-HGF)POF4-140
|0 G:(DE-HGF)POF4-141
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-100
|4 G:(DE-HGF)POF
|v Nukleare Entsorgung
|9 G:(DE-HGF)POF4-1411
|x 0
914 1 _ |y 2023
920 1 _ |0 I:(DE-Juel1)IEK-6-20101013
|k IEK-6
|l Nukleare Entsorgung
|x 0
920 1 _ |0 I:(DE-Juel1)ER-C-2-20170209
|k ER-C-2
|l Materialwissenschaft u. Werkstofftechnik
|x 1
980 _ _ |a poster
980 _ _ |a VDB
980 _ _ |a I:(DE-Juel1)IEK-6-20101013
980 _ _ |a I:(DE-Juel1)ER-C-2-20170209
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IFN-2-20101013


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