RESUMO
Fine clay particles have functioned as transport media for radiocesium in terrestrial environments after nuclear accidents. Because radiocesium is expected to be retained in clay minerals by a cation-exchange reaction, ascertaining trace cesium desorption behavior in response to changing solution conditions is crucially important. This study systematically investigated the desorption behavior of intrinsic Cs (13 nmol/g) in well-characterized Na-montmorillonite in electrolyte solutions (NaCl, KCl, CaCl2, and MgCl2) under widely differing cation concentrations (0.2 mM to 0.2 M). Batch desorption experiments demonstrated that Cs(+) desorption was inhibited significantly in the presence of the environmental relevant concentrations of Ca(2+) and Mg(2+) (>0.5 mM) and high concentrations of K(+). The order of ability for Cs desorption was Na(+) = K(+) > Ca(2+) = Mg(2+) at the highest cation concentration (0.2 M), which is opposite to the theoretical prediction based on the cation-exchange selectivity. Laser diffraction grain-size analyses revealed that the inhibition of Cs(+) desorption coincided with the increase of the clay tactoid size. Results suggest that radiocesium in the dispersed fine clay particles adheres on the solid phase when the organization of swelling clay particles occurs because of changes in solution conditions caused by both natural processes and artificial treatments.
Assuntos
Silicatos de Alumínio/química , Césio/isolamento & purificação , Silicatos/química , Adsorção , Bentonita/química , Cátions , Argila , Troca Iônica , Cinética , Minerais/análise , Tamanho da Partícula , SoluçõesRESUMO
Sediment trap observations of lakes in western Japan before and after Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident indicate that changes in the radioactive Cs discharge are influenced by fluctuations in precipitation and geomorphological conditions in each catchment. Contributions of FDNPP-derived (134,137)Cs to the sediment decreased from 19-48% to 10-15% within a few months, implying that the major transport processes of FDNPP-derived (134,137)Cs have changed from direct fallout to transport by soil particles.