The Adsorption of Perfluorooctane Sulfonate onto Sand, Clay, and Iron Oxide Surfaces

Fluorinated anionic surfactants have drawn considerable attention due to recent work showing significant concentrations in surface waters and biota from around the globe. A detailed understanding of the transport and fate of fluorinated surfactants through soil and like media must include an elucida...

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Bibliographic Details
Published inJournal of chemical and engineering data Vol. 52; no. 4; pp. 1165 - 1170
Main Authors Johnson, Ramona L, Anschutz, Amy J, Smolen, Jean M, Simcik, Matt F, Penn, R. Lee
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 01.07.2007
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Summary:Fluorinated anionic surfactants have drawn considerable attention due to recent work showing significant concentrations in surface waters and biota from around the globe. A detailed understanding of the transport and fate of fluorinated surfactants through soil and like media must include an elucidation of mineral surface chemistry. Five materials were equilibrated with solutions of perfluorooctane sulfonate (PFOS) to characterize adsorption:  kaolinite, Ottawa sand standard, synthetic goethite, Lake Michigan sediment, and iron-coated sand from Mappsville, VA. Aqueous and adsorbed PFOS was quantified with LC/MS (mass balance average:  101 ± 12 %, n = 37). The materials showed a near linear increase in adsorption as the equilibrium concentrations increased. Isotherms and calculated solid/solution distribution ratio experiments indicated that PFOS adsorption is significant but smaller than hydrocarbon analogues or organic compounds of similar molecular weight. Surface area normalized adsorption increased for the materials in the following order:  goethite < kaolinite < high iron sand < Ottawa sand standard. Experimental results and comparisons to published data suggest that organic carbon may play an important role in sorption whereas electrostatic attraction may play a role when organic carbon is not present.
Bibliography:ark:/67375/TPS-N51LWR23-9
istex:ECE8AAF0FECF6B5CF763EB67EB111F711E8586DB
ISSN:0021-9568
1520-5134
DOI:10.1021/je060285g