Anoxic iron electrocoagulation automatically modulates dissolved oxygen and pH for fast reductive decomplexation and precipitation of Cu(II)-EDTA: The critical role of dissolved Fe(II)

Fe-based replacement and precipitation are promising methods for removal of copper ethylenediaminetetraacetic acid (Cu(II)-EDTA) but are limited by the necessity of controlling pH and dissolved oxygen. The details of the decomplexation mechanism also remain unclear. The present work investigated an anoxic iron electro-coagulation process capable of automatically modulating anoxic conditions and solution pH during exposure to air and thus promoting the rapid and thorough decomplexation of Cu(II)-EDTA. Dissolved Fe (II), rather than Fe (II)-bearing minerals, was found to be primarily responsible for the reduction of Cu(II)-EDTA to Cu(I)-EDTA and for the subsequent replacement reaction to generate free Cu(I) ions within the initial pH range of 2-7. The Cu(I) was primarily precipitated as Cu2O on the surface of green rust and magnetite as the pH was increased. The aeration of these Fe-containing precipitates released free Cu(I) ions instead of chelated Cu into solution, allowing for recycling of the Cu. This release of Cu(I) was likely induced by the pH decrease during aeration. This study provides important insights regarding the reductive decomplexation of chelated Cu(II) and the recovery of Cu via anoxic iron electrocoagulation, which is a promising green approach to recycling Cu from wastewater.

Automated summary

This study investigates an anoxic iron electro-coagulation process that can automatically modulate anoxic conditions and solution pH to promote the rapid decomplexation of Cu(II)-EDTA. The dissolved Fe (II) is found to be responsible for the reduction of Cu(II)-EDTA to Cu(I)-EDTA and the subsequent replacement reaction. The Cu(I) is primarily precipitated as Cu2O on the surface of green rust and magnetite, and can be released into solution during aeration.