posted on 2005-10-15, 00:00authored byMatthew Ginder-Vogel, Thomas Borch, Melanie A. Mayes, Phillip M. Jardine, Scott Fendorf
Chromate is a widespread contaminant that has deleterious
impacts on human health, the mobility and toxicity of
which are diminished by reduction to Cr(III). While biological
and chemical reduction reactions of Cr(VI) are well
resolved, reduction within natural sediments, particularly
of arid environments, remains poorly described. Here, we
examine chromate reduction within arid sediments from
the Hanford, WA site, where Fe(III) (hydr)oxide and carbonate
coatings limit mineral reactivity. Chromium(VI) reduction
by Hanford sediments is negligible unless pretreated with
acid; acidic pretreatment of packed mineral beds having
a Cr(VI) feed solution results in Cr(III) associating with the
minerals antigorite and lizardite in addition to magnetite
and Fe(II)-bearing clay minerals. Highly alkaline conditions
(pH > 14), representative of conditions near high-level
nuclear waste tanks, result in Fe(II) dissolution and concurrent
Cr(VI) reduction. Additionally, Cr(III) and Cr(VI) are found
associated with portlandite, suggesting a secondary
mechanism for chromium retention at high pH. Thus, mineral
reactivity is limited within this arid environment and
appreciable reduction of Cr(VI) is restricted to highly alkaline
conditions resulting near leaking radioactive waste
disposal tanks.