Natürliche Schadstoffrückhalteprozesse für Arsen und Kupfer am Standort einer ehemaligen Buntfarbenfabrik

The sharply confined pattern of arsenic groundwater contamination at the site of a historic dye factory suggests that natural attenuation processes are active and efficient. The supporting data included sequential soil extractions combined with analyses of other soil properties like carbonate content, the loss of ignition and cation exchange capacity and the extraction characteristics of the original dye pigment. The results point to iron oxides and iron hydroxides as the most important adsorbers for copper and arsenic. The attenuation of copper can be estimated to be very efficient mainly due to its pH-controlled low solubility. Besides the specific adsorption to iron oxides, however, arsenic exhibits a rather large, loosely bound and easily exchangeable fraction. The speciation of arsenic in groundwater is dominated by As(V). The oxidation state of the original pigment is As(III). In some parts of the aquifer where suboxic conditions prevail, this oxidation state is conserved. In oxic zones of the aquifer, oxidation to the pentavalent form As(V) takes place.