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Selenide [Se(-II)] retention and mobilization in anoxic, iron-rich environments; Impacts of iron phase precipitation and transformation

Francisco, P. C. M.  ; Matsumura, Daiju   ; Kikuchi, Ryosuke*; Ishidera, Takamitsu ; Tachi, Yukio  

The radionuclide Selenium-79 (Se-79) is predicted to be a key contributor to the long-term radiologic hazards associated with geological high-level waste (HLW) repositories. Se exists predominantly as selenide Se(-II) under anoxic conditions in the deep subsurface, and is likely immobilized via precipitation with, or adsorption on, Fe(II) minerals. However, the initial immobilization mechanisms with metastable Fe(II) minerals, and Se(-II)s subsequent response to iron phase transformation in the long term remain poorly understood. In this work, we investigated the retention and mobilization behavior of Se(-II) as a function of pH and the mode of its initial interaction with aqueous or solid Fe(II) phases. We carried out batch precipitation and transformation experiments under N$$_{2}$$ atmosphere and reducing conditions. We examined two cases: in the first, Se(-II) was reacted with aqueous Fe(II), while in the second, Fe(OH)$$_{2}$$ was first precipitated before reaction with Se(-II); both experiments were carried out at pH 8 and 12. In both cases, Se(-II) introduction resulted in the immediate precipitation of black particles. EXAFS and TEM characterization showed that Se(-II) precipitated as iron selenide nanoparticles in both cases regardless of pH. Aging of these initial precipitates at $$^{90}$$C resulted in magnetite crystallization. Regardless of whether Se(-II) was reacted with aqueous Fe(II) or solid phases, it was completely retained as discrete, crystalline FeSe$$_{2}$$ at pH8. At pH12, Se(-II) was mostly remobilized; however, we observed evidence of partial retention via the precipitation of nanocrystalline iron selenide (Fe$$_{3}$$Se$$_{4}$$ or Fe$$_{7}$$Se$$_{8}$$) on the surface of magnetite, as well as by incorporation in defects on the edges of magnetite crystals. These results show that pH controls long-term Se(-II) behavior and that magnetite crystallization may play a role in the retention of Se(-II), particularly at high pH.

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