Pb(II) binding to humic substances: an equilibrium and spectroscopic study.

Environ Sci Technol

Instituto de Química Física de Materiales, Ambiente y Energía (INQUIMAE), y Departamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires , Buenos Aires, Argentina.

Published: August 2013

AI Article Synopsis

  • - The study investigates how lead (Pb(II)) binds to humic acids using various methods, including titrations and spectroscopy, to understand the interaction at a molecular level.
  • - Potentiometric titration indicates that Pb(II) has a bimodal affinity for humic acids, while fluorometric analysis suggests a simpler, monomodal affinity.
  • - Fluorescence analysis reveals that the binding of Pb(II) leads to the aggregation of humic substances, affecting their fluorescence, which is supported by IR spectroscopy results indicating complex interactions involving carboxylate groups.

Article Abstract

The binding of Pb(II) to humic acids is studied through an approach combining equilibrium and spectroscopic measurements. The methods employed are potentiometric and fluorometric titrations, fluorescence excitation-emission matrices (EEM) and IR spectroscopy. Potentiometric titration curves are analyzed using the NICA equations and an electrostatic model treating the humic particles as an elastic polyelectrolyte network. EEMs are analyzed using parallel factor analysis, decomposing the signal in its independent components and finding their dependence on Pb(II) activity. Potentiometric results are consistent with bimodal affinity distributions for Pb(II) binding, whereas fluorometric titrations are explained by monomodal distributions. EEM analysis is consistent with three independent components in the humic fluorescence response, which are assigned to moieties with different degree of aromaticity. All three components show a similar quenching behavior upon Pb(II) binding, saturating at relatively low Pb(II) concentrations. This is attributed to metal ion induced aggregation of humic molecules, resulting in the interaction between the aromatic groups responsible for fluorescence; this is also consistent with IR spectroscopy results. The observed behavior is interpreted considering that initial metal binding (observed as strongly binding sites), correspond to bi- or multidentate complexation to carboxylate groups, including binding between groups of different humic molecules, promoting aggregation; further metal ions (observed as weakly binding sites) bind to single ligand groups.

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Source
http://dx.doi.org/10.1021/es400999qDOI Listing

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