posted on 2005-05-02, 00:00authored byEugene S. Ilton, Anca Haiduc, Christopher L. Cahill, Andrew R. Felmy
High-resolution X-ray photoelectron spectroscopy was used to
demonstrate that reduction of aqueous U6+ at ferrous mica surfaces
at 25 °C preserves U5+ as the dominant sorbed species over a
broad range of solution compositions. Polymerization of sorbed
U5+ with sorbed U6+ and U4+ is identified as a possible mechanism
for how mineral surfaces circumvent the rapid disproportionation
of aqueous U5+. The general nature of this mechanism suggests
that U5+ could play an important, but previously unidentified, role
in the low-temperature chemistry of uranium in reducing, heterogeneous aqueous systems.