REVIEW: The fundamental mechanism of aqueous contaminant removal by metallic iron
Abstract
Contaminant co-precipitation with continuously generated and transformed iron corrosion products has received relatively little attention in comparison to other possible removal mechanisms (adsorption, oxidation, precipitation) in Fe0/H2O systems at near neutral pH values. A primary reason for this is that the use of elemental iron (Fe0) in environmental remediation is based on the thermodynamic-founded premise that reducible contaminants are potentially reduced while Fe 0 is oxidised. However, co-precipitation portends to be of fundamental importance for the process of contaminant removal in Fe 0/H2O systems, as the successful removal of bacteria, viruses and non reducible organic (e.g. methylene blue, triazoles) and inorganic (e.g. Zn) compounds has been reported. This later consideration has led to a search for the reasons why the importance of co-precipitation has almost been overlooked for more than a decade.
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