Partitioning Behavior of Per- and Polyfluoroalkyl Compounds between Pore Water and Sediment in Two Sediment Cores from Tokyo Bay, Japan
Publikation: Beiträge in Zeitschriften › Zeitschriftenaufsätze › Forschung › begutachtet
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in: Environmental Science & Technology, Jahrgang 43, Nr. 18, 15.09.2009, S. 6969-6975.
Publikation: Beiträge in Zeitschriften › Zeitschriftenaufsätze › Forschung › begutachtet
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TY - JOUR
T1 - Partitioning Behavior of Per- and Polyfluoroalkyl Compounds between Pore Water and Sediment in Two Sediment Cores from Tokyo Bay, Japan
AU - Ahrens, Lutz
AU - Yamashita, Nobuyoshi
AU - Yeung, Leo W. Y.
AU - Taniyasu, Sachi
AU - Horii, Yuichi
AU - Lam, Paul K. S.
AU - Ebinghaus, Ralf
PY - 2009/9/15
Y1 - 2009/9/15
N2 - The partitioning behavior of per- and polyfluoroalkyl compounds (PFCs) between pore water and sediment in two sediment cores collected from Tokyo Bay, Japan, was investigated. In addition, the fluxes and temporal trends in one dated sediment core were studied. Short-chain perfluoroalkyl carboxylic acids (PFCAs) (C ≤ 7) were found exclusively in pore water, while long-chain PFCAs (C ≥ 11) were found only in sediment. The perfluoroalkyl sulfonates (PFSAs), n-ethylperfluoro-1-octanesulfonamidoacetic acid (N-EtFOSAA), and perfluorooctane sulfonamide (PFOSA) seemed to bind more strongly to sediment than PFCAs. The enrichment of PFCs on sediment increased with increasing organic matter and decreasing pH. The perfluorocarbon chain length and functional group were identified as the dominating parameters that had an influence on the partitioning behavior of the PFCs in sediment. The maximum ΣPFC contamination in sediment was observed in 2001-2002 to be a flux of 197 pg cm -2 yr -1. Statistically significant increased concentrations in Tokyo Bay were found for perfluorooctanesulfonate (PFOS) (1956-2008), perfluorononanoic acid (PFNA) (1990-2008), and perfluoroundecanoic acid (PFUnDA) (1990-2008). Concentrations of PFOSA and N-EtFOSAA increased between 1985 and 2001, but after 2001, the concentration decreased significantly, which corresponded with the phase out of perfluorooctyl sulfonyl fluoride-based compounds by the 3M Company in 2000.
AB - The partitioning behavior of per- and polyfluoroalkyl compounds (PFCs) between pore water and sediment in two sediment cores collected from Tokyo Bay, Japan, was investigated. In addition, the fluxes and temporal trends in one dated sediment core were studied. Short-chain perfluoroalkyl carboxylic acids (PFCAs) (C ≤ 7) were found exclusively in pore water, while long-chain PFCAs (C ≥ 11) were found only in sediment. The perfluoroalkyl sulfonates (PFSAs), n-ethylperfluoro-1-octanesulfonamidoacetic acid (N-EtFOSAA), and perfluorooctane sulfonamide (PFOSA) seemed to bind more strongly to sediment than PFCAs. The enrichment of PFCs on sediment increased with increasing organic matter and decreasing pH. The perfluorocarbon chain length and functional group were identified as the dominating parameters that had an influence on the partitioning behavior of the PFCs in sediment. The maximum ΣPFC contamination in sediment was observed in 2001-2002 to be a flux of 197 pg cm -2 yr -1. Statistically significant increased concentrations in Tokyo Bay were found for perfluorooctanesulfonate (PFOS) (1956-2008), perfluorononanoic acid (PFNA) (1990-2008), and perfluoroundecanoic acid (PFUnDA) (1990-2008). Concentrations of PFOSA and N-EtFOSAA increased between 1985 and 2001, but after 2001, the concentration decreased significantly, which corresponded with the phase out of perfluorooctyl sulfonyl fluoride-based compounds by the 3M Company in 2000.
KW - Chemistry
KW - 3m companies
KW - Organic matter
KW - Perfluorocarbons
KW - Perfluorononanoic acids
KW - Perfluorooctane sulfonamide
KW - Perfluorooctane sulfonates
KW - Polyfluoroalkyl compounds
KW - Pore waters
KW - Sediment core
KW - Temporal trends
KW - Tokyo Bay
UR - http://www.scopus.com/inward/record.url?scp=70349099490&partnerID=8YFLogxK
U2 - 10.1021/es901213s
DO - 10.1021/es901213s
M3 - Journal articles
VL - 43
SP - 6969
EP - 6975
JO - Environmental Science & Technology
JF - Environmental Science & Technology
SN - 0013-936X
IS - 18
ER -