Radiation Damage Effects in Chlorite Investigated Using Microfocus Synchrotron Techniques

A detailed understanding of the mechanisms and effects of radiation damage in phyllosilicate minerals is a necessary component of the evaluation of the safety case for a deep geological disposal facility (GDF) for radioactive waste. Structural and chemical changes induced by α-particle damage will affect the performance of these minerals as reactive barrier materials (both in the near and far-field) over time scales relevant to GDF integrity. In this study, two examples of chlorite group minerals have been irradiated at α-particle doses comparable to those predicted to be experienced by the clay buffer material surrounding high-level radioactive waste canisters. Crystallographic aberrations induced by the focused 4He2+ ion beam are revealed via high-resolution, microfocus X-ray diffraction mapping. Interlayer collapse by up to 0.5 Å is prevalent across both macrocrystalline and microcrystalline samples, with the macrocrystalline specimen displaying a breakdown of the phyllosilicate structure into loosely connected, multioriented crystallites displaying variable lattice parameters. The damaged lattice parameters suggest a localized breakdown and collapse of the OH– rich, “brucite-like” interlayer. Microfocus Fe K-edge X-ray absorption spectroscopy illustrates this defect accumulation, manifest as a severe damping of the X-ray absorption edge. Subtle Fe2+/Fe3+ speciation changes are apparent across the damaged structures. A trend toward Fe reduction is evident at depth in the damaged structures at certain doses (8.76 × 1015 alpha particles/cm2). Interestingly, this reductive trend does not increase with radiation dose; indeed, at the maximum dose (1.26 × 1016 α particles/cm2) administered in this study, there is evidence for a slight increase in Fe binding energy, suggesting the development of a depth-dependent redox gradient concurrent with light ion damage. At the doses examined here, these damaged structures are likely highly reactive, as sorption capacity will, to an extent, be largely enhanced by lattice disruption and an increase in available “edge” sites.