The disposal of toxic metals [e.g., Cr(VI)] generated by the Department of
Energy during the cold war era has historically involved shallow land buria
l in unconfined pits and trenches. The objectives of this study were to inv
estigate the impact of coupled hydrologic and geochemical processes on the
fate and transport of Cr(VI) in undisturbed soil cores obtained from a frac
tured, acidic inceptisol that are commonly used in the disposal of waste at
the Oak Ridge National Laboratory. The mobility of Cr(VI) was significantl
y retarded relative to a nonreactive Br- tracer, and the mobility decreased
with increased loading of the solid phase with natural organic matter (NOM
). A significant portion of added Cr(VI) did not elute from the columns, an
d X-ray absorption near-edge structure (XANES) revealed that both Cr(VI) an
d Cr(III) resided on the sail mineral surfaces. The reduction of Cr(VI) to
Cr(III) was dramatically more significant on soils with higher levels of su
rface-bound NOM. This indicated that NOM was serving as a suitable reductan
t during Cr(VI) transport even in the presence of potentially competing geo
chemical oxidation reactions involving Cr. The redox reaction was catalyzed
by the presence of soil mineral surfaces, and the reduced product Cr(III)
was immobilized as a tightly bound moiety. The effectiveness of surface-bou
nd NOM to reduce toxic Cr(VI) to Cr(III) under acidic conditions has import
ant implications regarding the design and implementation of in situ remedia
l strategies.