Rates of hydrogen peroxide decomposition, hydroxyl radical production, and
oxygen evolution were investigated in silica sand-goethite slurries using u
nstabilized and stabilized hydrogen peroxide formulations. The goethite-cat
alyzed decomposition of unstabilized hydrogen peroxide formulations resulte
d in more rapid hydrogen peroxide loss and oxygen evolution relative to sys
tems containing a highly stabilized hydrogen peroxide formulation. Systems
at neutral pH and those containing higher goethite concentrations were char
acterized by higher rates of hydrogen peroxide decomposition and by more ox
ygen evolution. The stabilized hydrogen peroxide formulation showed greater
hydroxyl radical production relative to the unstabilized formulations. Fur
thermore, hydroxyl radical production rates were greater at neutral pH than
at the acidic pH regimes. The results suggest that when stabilized hydroge
n peroxide is injected into the subsurface during in situ bioremediation, n
aturally occurring minerals such as goethite may initiate Fenton-like react
ions. While these reactions may prove to be toxic to microorganisms, they h
ave the potential to chemically oxidize contaminants in soils and groundwat
er. (C) 1999 Elsevier Science B.V. All rights reserved.