Role of EDTA protonation in chelation-based removal of mercury ions from water

Abstract

A robust method of hazardous metal ion removal from an aqueous environment involves the use of chelating agents, such as ethylenediaminetetraacetic acid (EDTA). Here, we focus on mercury (Hg²⁺) uptake by EDTA using both molecular dynamics and density functional theory simulations. Our results indicate that the deprotonation of the EDTA carboxylate groups improves the localization of negative charge on the deprotonated sites. This mechanism facilitates charge transfer between the metal ions and EDTA, and provides a stronger and more stable EDTA–Hg²⁺ complex formation improving the efficiency of the chelation process. The best metal removal conditions are achieved using the fully deprotonated form of EDTA, which naturally occurs at pH levels above 3.