An anaerobic field injection experiment in a landfill leachate plume, Grindsted, Denmark 1. Experimental setup, tracer movement, and fate of aromaticand chlorinated compounds
K. Rugge et al., An anaerobic field injection experiment in a landfill leachate plume, Grindsted, Denmark 1. Experimental setup, tracer movement, and fate of aromaticand chlorinated compounds, WATER RES R, 35(4), 1999, pp. 1231-1246
A continuous, natural-gradient field injection experiment, involving 18 xen
obiotic compounds and bromide as tracers, was performed in the anaerobic re
gion of a leachate plume downgradient from the Grindsted Landfill, Denmark.
The injection lasted for 195 days, and within this period a continuous clo
ud was established. Over a period of 924 days the cloud movement was monito
red in approximately 70 discrete sampling points in the central part of the
cloud, and the spatial distribution was described by seven cloud snapshots
involving 400-700 sampling points. The bromide cloud movement closely foll
owed the varying flow direction predicted by the water table measurements.
Moment analysis showed decreasing tracer flow velocities and reduced captur
e of bromide mass with time, which may be explained by varying flow conditi
ons (direction, hydraulic gradient) and the heterogeneous geological condit
ions in the sandy aquifer. Naphthalene, having the highest log K-ow value,
was the most retarded compound, with a retardation of less than 10%. Theref
ore sorption was not considered to be a significant attenuation process for
any of the compounds studied. Transformation under iron-reducing condition
s was observed for toluene, o-xylene, TeCM, 1,1,1-TCA, PCE, and TCE, while
transformation of benzene and napthalene was not detected in the aquifer wi
thin the time frame of this study. First-order transformation rates were in
the range of 0.028-0.039 d(-1) and 0.0014-0.0028 d(-1) for the aromatic co
mpounds toluene and o-xylene, respectively. The rates for the chlorinated a
liphatic compounds, tetrachloromethane, 1,1,1-trichloroethane, tetrachloroe
thylene, and trichloroethylene, were >0.7 d(-1), 0.0044-0.0054 d(-1), 0.001
2-0.0038 d(-1), and 0.0003-0.001 d(-1), respectively. Long lag periods and
slow transformation rates were observed for some of the compounds, suggesti
ng that lack of transformation reported in the literature may be attributab
le to short experimental periods in those studies.