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Impact of Variable Water Chemistry on PFOS-Goethite Interactions: Experimental Evidence and Surface Complexation
Jacopo Cogorno1,2, Massimo Rolle1,3
1Department of Environmental and Resource Engineering, Technical University of Denmark, Miljøvej, Building 115, 2800 Kgs. Lyngby, Denmark.
Perfluorooctanesulfonate (PFOS) binds to goethite via hydrogen bonds and outer-sphere complexes. Solution chemistry, like pH and ionic strength, significantly influences these binding mechanisms, affecting PFOS environmental fate.
Area of Science:
- Environmental Chemistry
- Geochemistry
- Surface Chemistry
Background:
- Perfluorooctanesulfonate (PFOS) is a persistent environmental contaminant with significant toxic effects.
- Understanding PFOS interactions with mineral surfaces is crucial for predicting its environmental behavior.
Purpose of the Study:
- To investigate the sorption mechanisms of PFOS on goethite surfaces.
- To determine the impact of varying water chemistry (pH, ionic strength) on PFOS sorption.
Main Methods:
- Sorption experiments with controlled pH, ionic strength, and PFOS concentration.
- Infrared (IR) spectroscopy for surface analysis.
- Surface complexation modeling to elucidate binding mechanisms.
Main Results:
- PFOS binds to goethite through strong hydrogen-bonded (HB) complexes and weaker outer-sphere complexes (OS-Na+).
- Acidic conditions and low ionic strength favor HB complex formation.
- Higher electrolyte concentrations and pH promote ternary PFOS-Na+-goethite outer-sphere complex formation.
Conclusions:
- Solution chemistry critically controls PFOS adsorption onto mineral surfaces.
- Accurate prediction of PFOS mobility requires surface complexation models incorporating mechanistic details.
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