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  • Comparison of the sorption behaviors and mechanisms of perfluorosulfonates and perfluorocarboxylic acids on three kinds of clay minerals.

Comparison of the sorption behaviors and mechanisms of perfluorosulfonates and perfluorocarboxylic acids on three kinds of clay minerals.

Chemosphere (2014-08-13)
Lixia Zhao, Jingna Bian, Yahui Zhang, Lingyan Zhu, Zhengtao Liu
ABSTRACT

The sorption of four perfluoroalkyl acids (PFAAs) [perfluorooctane sulfonate (PFOS), perfluorohexane sulfonate (PFHxS), perfluorooctanoic acid (PFOA) and perfluorohexanoic acid (PFHxA)] on three typical minerals [montmorillonite (MM), kaolinite (KL) and hematite (HM)] was studied. The sorption of PFOS and PFHxS was much stronger than PFOA and PFHxA. The sorption of each PFAA on the minerals followed an order of HM>KL>MM, even though MM was positively while KL and HM were negatively charged, implying that the sorption is driven by some other interactions besides electrostatic attraction. The sorption decreased with an increase in pH and a decrease in ionic strength of the solution, and their impacts on PFOS were much stronger than other three PFAAs. Surface complexing and hydrogen-bonding could make great contributions to the sorption of PFOS on the minerals. The results are important for understanding the transport and fate of PFAAs in sediment and ground water.

MATERIALI
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Iron(III) oxide, powder, <5 μm, ≥96%
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Perfluorooctanoic acid, 95%
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Bentonite
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Halloysite Nanoclay
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Iron(III) oxide, nanopowder, <50 nm particle size (BET)
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Iron(III) oxide, ≥99.995% trace metals basis
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Nanoclay hydrophilic bentonite
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Kaolin
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Pentadecafluorooctanoic acid ammonium salt, ≥98.0% (NT)
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Heptadecafluorooctanesulfonic acid solution, 100 μg/mL in methanol, analytical standard
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Iron(III) oxide, dispersion, nanoparticles, ≤110 nm particle size, 15 wt. % in ethanol
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Pentadecafluorooctanoic acid, analytical standard
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Kaolin, meets USP testing specifications
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Pentadecafluorooctanoic acid solution, 100 μg/mL in methanol, analytical standard
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Kaolin, heavy, powder
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Kaolin, tested according to Ph. Eur.