Sources, fate and transport of perfluorocarboxylates

被引:2034
作者
Prevedouros, K
Cousins, IT [1 ]
Buck, RC
Korzeniowski, SH
机构
[1] Stockholm Univ, Dept Appl Environm Sci, ITM, SE-10691 Stockholm, Sweden
[2] EI duPont & Nemours & Co Inc, Wilmington, DE 19880 USA
关键词
D O I
10.1021/es0512475
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This review describes the sources, fate, and transport of perfluorocarboxylates (PFCAs) in the environment, with a specific focus on perfluorooctanoate (PFO). The global historical industry-wide emissions of total PFCAs from direct (manufacture, use, consumer products) and indirect (PFCA impurities and/or precursors) sources were estimated to be 3200-7300 tonnes. It was estimated that the majority (similar to 80%) of PFCAs have been released to the environment from fluoropolymer manufacture and use. Although indirect sources were estimated to be much less important than direct sources,there were larger uncertainties associated with the calculations for indirect sources. The physical-chemical properties of PFO (negligible vapor pressure, high solubility in water, and moderate sorption to solids) suggested that PFO would accumulate in surface waters. Estimated mass inventories of PFO in various environmental compartments confirmed that surface waters, especially oceans, contain the majority of PFO. The only environmental sinks for PFO were identified to be sediment burial and transport to the deep oceans, implying a long environmental residence time. Transport pathways for PFCAs in the environment were reviewed, and it was concluded that, in addition to atmospheric transport/degradation of precursors, atmospheric and ocean water transport of the PFCAs themselves could significantly contribute to their long-range transport. It was estimated that 2-12 tonnes/ year of PFO are transported to the Artic by oceanic transport, which is greater than the amount estimated to result from atmospheric transport/degradation of precursors.
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页码:32 / 44
页数:13
相关论文
共 152 条
[31]  
DEVOOGT P, 2005, ORGANOHALOGEN COMPD, V67, P790
[32]   Fluorotelomer alcohol biodegradation yields poly- and perfluorinated acids [J].
Dinglasan, MJA ;
Ye, Y ;
Edwards, EA ;
Mabury, SA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (10) :2857-2864
[33]   Atmospheric aerosols as prebiotic chemical reactors [J].
Dobson, CM ;
Ellison, GB ;
Tuck, AF ;
Vaida, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :11864-11868
[34]  
*DUP COMP, 2004, OV APFO TEL ACT DUPO
[35]  
*DUP COMP, 2003, 200300120217 OPPT US
[36]  
*DUP COMP, 2005, DUP GLOB PFOA STRAT
[37]  
DYNEON, 2004, NUTZEN FLUORKUNSTSTO
[38]   Atmospheric lifetime of fluorotelomer alcohols [J].
Ellis, DA ;
Martin, JW ;
Mabury, SA ;
Hurley, MD ;
Andersen, MPS ;
Wallington, TJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (17) :3816-3820
[39]   Degradation of fluorotelomer alcohols: A likely atmospheric source of perfluorinated carboxylic acids [J].
Ellis, DA ;
Martin, JW ;
De Silva, AO ;
Mabury, SA ;
Hurley, MD ;
Andersen, MPS ;
Wallington, TJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (12) :3316-3321
[40]  
Ellis DA, 2002, HANDB ENVIRON CHEM, V3, P63