Abstract
The mechanism of aqueous contaminant removal by elemental (Fe 0 ) materials (e.g., in Fe 0 -H2O systems) has been largely discussed in the iron technology literature. Two major removal mechanisms are usually discussed: (i) contaminant adsorption onto Fe 0 oxidation products, and (ii) contaminant reduction by Fe 0 , Fe II or H/H2. However, a closer inspection of the chemistry of the Fe 0 -H2O system reveals that co-precipitation could be the primary removal mechanism. The plausibility of contaminant co-precipitation with corrosion products as independent contaminant re- moval mechanism is discussed here. It shows that the current concept does not take into account that the corrosion product generation is a dynamic process in the course of which contaminants are entrapped in the matrix of hydroxides. It is recalled that contaminant co-precipitation with hydroxides/oxides is an unspecific removal mechanism. Contaminant co-precipitation as primary removal mechanism is compatible with subsequent reduction and explains why redox- insensitive species are quantitatively removed. Adsorption and co-precipitation precede reduction and abiotic reduction, when it takes place, occurs independently by a direct (electrons from Fe 0 ) or an indirect (electrons from Fe II /H2) mecha- nism.
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