Comparing the Pb(II) binding with different fluorescent components of dissolved organic matter from typical sources

Abstract

Dissolved organic matter (DOM) is important for determining the speciation, environmental behavior, and effects of metal pollutants in aquatic environments. However, little is known about the difference between DOM from natural and anthropogenic sources for binding Pb(II). This study examined the Pb(II) binding with DOM from four typical sources including river, leaf litter leachate, and the influent and effluent of a wastewater treatment plant, using fluorescence quenching titration and excitation-emission matrices-parallel factor analysis (EEMs-PARAFAC). Four humic-like and one protein-like fluorescent components were identified, with much higher protein-like fraction and lower humification degree for the influent than for other sources. In the river water and leaf litter leachate, the abundant humic-like components were quenched by 6-17% while the protein-like component kept stable (2-4%) by the addition of Pb(II). In contrast, the influent DOM showed stronger fluorescence quenching of the protein-like component (46%) with higher conditional stability constant and binding fraction of fluorophore than the humic-like components (15-21%). The effluent DOM displayed weak quenching for all fluorescent components (4-6%) and thus weak complexation with Pb(II), indicating notable changes in the chemical composition and metal-binding affinity of DOM by wastewater treatments. These results demonstrated significant impacts of DOM source and chemical composition on its Pb(II) complexation properties, which have implications for understanding the interactions between DOM and heavy metals.

Keywords: Dissolved organic matter; EEMs-PARAFAC; Fluorescence quenching titration; Heavy metal; Pb(II).