TY - JOUR
T1 - Biogeochemical processes at the fringe of a landfill leachate pollution plume: potential for dissolved organic carbon, Fe(II), Mn(II), NH 4, and CH 4 oxidation
AU - van Breukelen, Boris M.
AU - Griffioen, Jasper
PY - 2004
Y1 - 2004
N2 - Various redox reactions may occur at the fringe of a landfill leachate
plume, involving oxidation of dissolved organic carbon (DOC), CH
4, Fe(II), Mn(II), and NH 4 from leachate and
reduction of O 2, NO 3 and SO 4 from
pristine groundwater. Knowledge on the relevance of these processes is
essential for the simulation and evaluation of natural attenuation (NA)
of pollution plumes. The occurrence of such biogeochemical processes was
investigated at the top fringe of a landfill leachate plume (Banisveld,
the Netherlands). Hydrochemical depth profiles of the top fringe were
captured via installation of a series of multi-level samplers at 18, 39
and 58 m downstream from the landfill. Ten-centimeter vertical
resolution was necessary to study NA within a fringe as thin as 0.5 m.
Bromide appeared an equally well-conservative tracer as chloride to
calculate dilution of landfill leachate, and its ratio to chloride was
high compared to other possible sources of salt in groundwater. The
plume fringe rose steadily from a depth of around 5 m towards the
surface with a few meters in the period 1998-2003. The plume uplift may
be caused by enhanced exfiltration to a brook downstream from the
landfill, due to increased precipitation over this period and an
artificial lowering of the water level of the brook. This rise invoked
cation exchange including proton buffering, and triggered degassing of
methane. The hydrochemical depth profile was simulated in a 1D vertical
reactive transport model using PHREEQC-2. Optimization using the
nonlinear optimization program PEST brought forward that solid organic
carbon and not clay minerals controlled retardation of cations. Cation
exchange resulted in spatial separation of Fe(II), Mn(II) and NH
4 fronts from the fringe, and thereby prevented possible
oxidation of these secondary redox species. Degradation of DOC may
happen in the fringe zone. Re-dissolution of methane escaped from the
plume and subsequent oxidation is an explanation for absence of
previously present nitrate and anaerobic conditions in pristine
groundwater above the plume. Stable carbon isotope (δ
13C) values of methane confirm anaerobic methane oxidation
immediately below the fringe zone, presumably coupled to reduction of
sulfate, desorbed from iron oxide. Methane must be the principle
reductant consuming soluble electron-acceptors in pristine groundwater,
thereby limiting NA for other solutes including organic micro-pollutants
at the fringe of this landfill leachate plume.
AB - Various redox reactions may occur at the fringe of a landfill leachate
plume, involving oxidation of dissolved organic carbon (DOC), CH
4, Fe(II), Mn(II), and NH 4 from leachate and
reduction of O 2, NO 3 and SO 4 from
pristine groundwater. Knowledge on the relevance of these processes is
essential for the simulation and evaluation of natural attenuation (NA)
of pollution plumes. The occurrence of such biogeochemical processes was
investigated at the top fringe of a landfill leachate plume (Banisveld,
the Netherlands). Hydrochemical depth profiles of the top fringe were
captured via installation of a series of multi-level samplers at 18, 39
and 58 m downstream from the landfill. Ten-centimeter vertical
resolution was necessary to study NA within a fringe as thin as 0.5 m.
Bromide appeared an equally well-conservative tracer as chloride to
calculate dilution of landfill leachate, and its ratio to chloride was
high compared to other possible sources of salt in groundwater. The
plume fringe rose steadily from a depth of around 5 m towards the
surface with a few meters in the period 1998-2003. The plume uplift may
be caused by enhanced exfiltration to a brook downstream from the
landfill, due to increased precipitation over this period and an
artificial lowering of the water level of the brook. This rise invoked
cation exchange including proton buffering, and triggered degassing of
methane. The hydrochemical depth profile was simulated in a 1D vertical
reactive transport model using PHREEQC-2. Optimization using the
nonlinear optimization program PEST brought forward that solid organic
carbon and not clay minerals controlled retardation of cations. Cation
exchange resulted in spatial separation of Fe(II), Mn(II) and NH
4 fronts from the fringe, and thereby prevented possible
oxidation of these secondary redox species. Degradation of DOC may
happen in the fringe zone. Re-dissolution of methane escaped from the
plume and subsequent oxidation is an explanation for absence of
previously present nitrate and anaerobic conditions in pristine
groundwater above the plume. Stable carbon isotope (δ
13C) values of methane confirm anaerobic methane oxidation
immediately below the fringe zone, presumably coupled to reduction of
sulfate, desorbed from iron oxide. Methane must be the principle
reductant consuming soluble electron-acceptors in pristine groundwater,
thereby limiting NA for other solutes including organic micro-pollutants
at the fringe of this landfill leachate plume.
M3 - Article
SN - 0169-7722
VL - 73
SP - 181
EP - 205
JO - Journal of Contaminant Hydrology
JF - Journal of Contaminant Hydrology
IS - 1
ER -