Abstract

An overview is presented on possible mechanisms that control the leaching behaviour of the oxyanion forming elements As, Cr, Mo, Sb, Se, V and W in cementituous systems and alkaline solid wastes, such as municipal solid waste incinerator bottom ash, fly ash and air pollution control residues, coal fly ash and metallurgical slags. Although the leachability of these elements generally depends on their redox state, speciation measurements are not common. Therefore, experimental observations available in the literature are combined with a summary of the thermal behaviour of these elements to assess possible redox states in freshly produced alkaline wastes, given their origin at high temperature. Possible redox reactions occurring at room temperature, on the other hand, are reviewed because these may alter the initial redox state in alkaline wastes and their leachates. In many cases, precipitation of oxyanions as a pure metalate cannot provide a satisfactory explanation for their leaching behaviour. It is therefore highly likely that adsorption and solid solution formation with common minerals in alkaline waste and cement reduce the leachate concentration of oxyanions below pure-phase solubility. (c) 2008 Elsevier Ltd. All rights reserved.

Published in

Applied Geochemistry
2008, Volume: 23, number: 5, pages: 955-976
Publisher: PERGAMON-ELSEVIER SCIENCE LTD

UKÄ Subject classification

Geochemistry


Publication identifier

DOI: https://doi.org/10.1016/j.apgeochem.2008.02.001

Permanent link to this page (URI)

https://res.slu.se/id/publ/80968