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Role of Electrochemical Surface Potential and Irradiation on Garnet-Type Almandine’s Dissolution Kinetics

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Nanoscale-resolved quantifications of almandine’s (Fe3Al2(SiO4)3) dissolution rates across a range of pHs (1 ≤ pH ≤ 13)—established using vertical scanning interferometry—reveal that its dissolution rate achieves a minimum around pH… Click to show full abstract

Nanoscale-resolved quantifications of almandine’s (Fe3Al2(SiO4)3) dissolution rates across a range of pHs (1 ≤ pH ≤ 13)—established using vertical scanning interferometry—reveal that its dissolution rate achieves a minimum around pH 5. This minimum coincides with almandine’s point of zero charge. These trends in almandine’s dissolution can be estimated using the Butler–Volmer equation that reveals linkages between surface potentials and dissolution rates, demonstrating proton- and hydroxyl-promoted breakage of Si–O bonds. In contrast to well-polymerized silicates, the dissolution of almandine can also occur through the rupture of its cationic bonds. This behavior is reflected in the observed influences of irradiation on its dissolution kinetics. Molecular dynamics simulations highlight that irradiation induces alterations in the atomic structure of almandine by reducing the coordination state of the cations (Fe2+ and Al3+), thereby enhancing its reactivity by a factor of two. This is consistent with the m...

Keywords: irradiation; surface; almandine dissolution; dissolution; almandine; dissolution kinetics

Journal Title: Journal of Physical Chemistry C
Year Published: 2018

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