22 results on '"Russell, Mark H."'
Search Results
2. Evaluation of PFO formation from the biodegradation of a fluorotelomer-based urethane polymer product in aerobic soils
- Author
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Russell, Mark H., Berti, William R., Szostek, Bogdan, Wang, Ning, and Buck, Robert C.
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- 2010
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3. A site-specific screening comparison of modeled and monitored air dispersion and deposition for perfluorooctanoate
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Barton, Catherine A., Zarzecki, Charles J., and Russell, Mark H.
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Soil acidification -- Research ,Air quality -- Models ,Perfluorocarbons -- Research ,Environmental services industry ,Environmental issues ,Science and technology - Abstract
ABSTRACT This work assessed the usefulness of a current air quality model (American Meteorological Society/Environmental Protection Agency Regulatory Model [AERMOD]) for predicting air concentrations and deposition of perfluorooctanoate (PFO) near [...]
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- 2010
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4. Inhalation and oral toxicokinetics of 6:2 FTOH and its metabolites in mammals.
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Russell, Mark H., Himmelstein, Matthew W., and Buck, Robert C.
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METABOLITES , *MAMMAL physiology , *FLUOROTELOMER alcohols , *BIOLOGICAL monitoring , *LIVER cells - Abstract
The toxicokinetics of 6:2 fluorotelomer alcohol (6:2 FTOH) and its terminal perfluorinated and polyfluorinated metabolites (PFBA, PFHxA, PFHpA and 5:3 Acid) have been calculated from laboratory studies of rats and from a biomonitoring study of humans. In vitro studies with mouse, rat and human hepatocytes indicate qualitatively similar metabolic pathways of 6:2 FTOH. In a one-day inhalation study of 6:2 FTOH in rats, PFBA, PFHxA, PFHpA and 5:3 Acid were determined to be the major metabolites in plasma with calculated elimination half-lives of 1.3–15.4 h and metabolic yields up to 2.7 mol%. In five-day and 23-day inhalation studies and a 90-day oral study of 6:2 FTOH, the plasma or serum concentration profile of 5:3 Acid was several-fold higher than concentrations observed in the single day study, resulting in an estimated elimination half-life of 20–30 d. In contrast, the concentrations of PFBA, PFHxA and PFHpA showed little or no concentration increase with repeated exposure. Elimination half-lives of PFHxA, PFHpA and 5:3 Acid in humans were estimated from a study of professional ski wax technicians who were occupationally exposed to aerosolized and volatilized components of fluorinated glide wax. The resulting human elimination half-life values of PFHxA, PFHpA and 5:3 Acid were 32, 70 and 43 d, respectively. Based on a one compartment toxicokinetic model, current environmental air concentrations of 6:2 FTOH are estimated to result in plasma concentrations of PFHxA, PFHpA and 5:3 Acid that are less than or equal to typical LOQ values, in agreement with extant biomonitoring results. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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5. Elimination kinetics of perfluorohexanoic acid in humans and comparison with mouse, rat and monkey.
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Russell, Mark H., Nilsson, Helena, and Buck, Robert C.
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CAPROATES , *ELIMINATION reaction kinetics , *COMPARATIVE studies , *LABORATORY rodents , *LABORATORY monkeys , *ANIMAL species , *HEALTH risk assessment , *BODY weight - Abstract
Highlights: [•] Elimination half-life of PFHxA determined from blood of ski wax technicians. [•] Geomean human elimination half-life of PFHxA is 32d (range 14–49d). [•] Elimination half-life of PFHxA in mammalian species is proportional to body weight. [•] Rate of PFHxA elimination from mammals is useful for subsequent risk assessment. [ABSTRACT FROM AUTHOR]
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- 2013
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6. Good modeling practice guidelines for applying multimedia models in chemical assessments.
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Buser, Andreas M, MacLeod, Matthew, Scheringer, Martin, Mackay, Don, Bonnell, Mark, Russell, Mark H, DePinto, Joseph V, and Hungerbühler, Konrad
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DECISION making ,RISK assessment of hazardous substances ,CHEMICAL engineering ,CHEMICAL models ,UNCERTAINTY (Information theory) ,DATA analysis - Abstract
Multimedia mass balance models of chemical fate in the environment have been used for over 3 decades in a regulatory context to assist decision making. As these models become more comprehensive, reliable, and accepted, there is a need to recognize and adopt principles of Good Modeling Practice (GMP) to ensure that multimedia models are applied with transparency and adherence to accepted scientific principles. We propose and discuss 6 principles of GMP for applying existing multimedia models in a decision-making context, namely 1) specification of the goals of the model assessment, 2) specification of the model used, 3) specification of the input data, 4) specification of the output data, 5) conduct of a sensitivity and possibly also uncertainty analysis, and finally 6) specification of the limitations and limits of applicability of the analysis. These principles are justified and discussed with a view to enhancing the transparency and quality of model-based assessments. Integr Environ Assess Manag 2012; 8: 703-708. © 2012 SETAC [ABSTRACT FROM AUTHOR]
- Published
- 2012
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7. TFA from HFO-1234yf: Accumulation and aquatic risk in terminal water bodies.
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Russell, Mark H., Hoogeweg, Gerco, Webster, Eva M., Ellis, David A., Waterland, Robert L., and Hoke, Robert A.
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TRIFLUOROACETIC acid , *BODIES of water , *GEOGRAPHIC information systems , *EVAPORATION (Chemistry) - Abstract
A next-generation mobile automobile air-conditioning (MAC) refrigerant, HFO-1234yf (CF3CF = CH2), is being developed with improved environmental characteristics. In the atmosphere, it ultimately forms trifluoroacetic acid (TFA(A); CF3COOH), which is subsequently scavenged by precipitation and deposited on land and water as trifluoroacetate (TFA; CF3COO-). Trifluoroacetate is environmentally stable and has the potential to accumulate in terminal water bodies, that is, aquatic systems receiving inflow but with little or no outflow and with high rates of evaporation. Previous studies have estimated the emission rates of HFO-1234yf and have modeled the deposition concentrations and rates of TFA across North America. The present study uses multimedia modeling and geographic information system (GIS)-based modeling to assess the potential concentrations of TFA in terminal water bodies over extended periods. After 10 years of emissions, predicted concentrations of TFA in terminal water bodies across North America are estimated to range between current background levels (i.e., 0.01-0.22 µg/L) and 1 to 6 µg/L. After 50 years of continuous emissions, aquatic concentrations of 1 to 15 µg/L are predicted, with extreme concentrations of up to 50 to 200 µg/L in settings such as the Sonoran Desert along the California/Arizona (USA) border. Based on the relative insensitivity of aquatic organisms to TFA, predicted concentrations of TFA in terminal water bodies are not expected to impair aquatic systems, even considering potential emissions over extended periods. Environ. Toxicol. Chem. 2012; 31: 1957-1965. © 2012 SETAC [ABSTRACT FROM AUTHOR]
- Published
- 2012
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8. MODELING THE ENVIRONMENTAL FATE OF PERFLUOROOCTANOATE AND ITS PRECURSORS FROM GLOBAL FLUOROTELOMER ACRYLATE POLYMER USE.
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VAN ZELM, ROSALIE, HUIJBREGTS, MARK A.J., RUSSELL, MARK H., JAGER, TJALLING, and VAN DE MEENT, DIK
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PERFLUOROOCTANOIC acid ,SURFACE active agents ,FLUOROCARBONS ,ANIONS ,ACRYLATES ,POLYMERS - Abstract
The environment contains various direct and indirect sources of perfluorooctanoic acid (PFOA). The present study uses a dynamic multispecies environmental fate model to analyze the potential formation of perfluorooctanoate (PFO), the anion of PFOA, in the environment from fluorotelomer acrylate polymer (FTacrylate) emitted to landfills and wastewater, residual fluorotelomer alcohol (8:2 FTOH) in FTacrylate, and residual PFOA in FTacrylate. A multispecies version of the SimpleBox model, which is capable of determining the fate of a chemical and its degradation products, was developed for this purpose. An uncertainty analysis on the chemical-specific input parameters was performed to examine for uncertainty in modeled concentrations. In 2005, residual 8:2 FTOH made up 80% of the total contribution of FTacrylate use to PFO concentrations in global oceans, and residual PFOA in FTacrylate contributed 15% to PFO concentrations from FTacrylate use in global oceans. After hundreds of years, however, the main source of PFO from total historical FTacrylate production is predicted to be FTacrylate degrading in soil following land application of sludge from sewage treatment plants, followed by FTacrylate still present in landfills. Uncertainty in modeled PFO concentrations was up to a factor of 3.3. Current FTacrylate use contributes less than 1% of the PFO in seawater, but because direct PFOA emission sources are reduced and PFOA continues to be formed from FTacrylate in soil and in landfills, this fraction grows over time. [ABSTRACT FROM AUTHOR]
- Published
- 2008
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9. Are PFCAs Bioaccumulative? A Critical Review and Comparison with Regulatory Criteria and Persistent Lipophilic Compounds.
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Conder, Jason M., Hoke, Robert A., de Wolf, Watze, Russell, Mark H., and Buck, Robert C.
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- 2008
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10. Investigation of the Biodegradation Potential of a Fluoroacrylate Polymer Product in Aerobic Soils.
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Russell, Mark H., Berti, William R., Szostek, Bogdan, and Buck, Robert C.
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ENVIRONMENTAL research , *AEROBIC bacteria , *SOIL composition , *ENVIRONMENTAL soil science , *BIODEGRADATION , *CHEMICAL decomposition , *BIOCHEMISTRY , *MICROBIOLOGY , *ALCOHOL - Abstract
Biodegradation of fluorinated polymers is of interest to assess them as a potential source of perfluorocarboxylates (PFCAs) in the environment A fluoroacrylate polymer product test substance was studied in four aerobic soils over two years to assess whether the fluorotelomer alcohol (FTOH) side chains covalently bonded to the polymer backbone may be transformed to form PFCAs. The test substance itself was not directly measured; instead, nine analytes were determined to evaluate biodegradation. Terminal biotransformation products measured included periluorooctanoate (PFO), perfluorononanoate (PFN), perfluorodecanoate (PFD), pertluoroundecanoate (PFU), and pentadecafluorodecanoate (7-3 acid). The molar concentration of 8-2 fluorotelomer alcohol (8-2 FTOH) in the test substance, fluoroacrylate polymer and residual unreacted raw materials and impurities ("residuals") were compared with the molar concentrations of the terminal biotransformation products for mass balance and kinetic assessments. Over the two year time frame of the experimental study, the fluoroacrylate polymer showed a slight extent of potential biodegradation under the experimental conditions of the study. A biodegradation half-life of 1200-1700 years was calculated for the fluoroacrylate polymer based on the rate of formation of PFO in aerobic soils. When the degradation rates of the fluoroacrylate polymer and residuals were applied to estimated total historic fluoroacrylate polymer production, use and disposal,the biodegradation of fluoroacrylate polymer and residuals is calculated to contribute less than 5 tonnes of PFO per year globally to PFCAs present in the environment. [ABSTRACT FROM AUTHOR]
- Published
- 2008
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11. High-Resolution Atmospheric Modeling of Fluorotelomer Alcohols and Perfluorocarboxylic Acids in the North American Troposphere.
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Yarwood, Greg, Kemball-Cook, Susan, Keinath, Michael, Waterland, Robert L., Korzeniowski, Stephen H., Buck, Robert C., Russell, Mark H., and Washburn, Stephen T.
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- 2007
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12. Modeling Global-Scale Fate and Transport of Perfluorooctanoate Emitted from Direct Sources.
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Armitage, James, Cousins, Ian T., Buck, Robert C., Prevedouros, Konstantinos, Russell, Mark H., Macleod, Matthew, and Korzeniowskit, Stephen H.
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- 2006
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13. Uncalibrated modelling of conservative tracer and pesticide leaching to groundwater: comparison of potential Tier II exposure assessment models.
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Fox, Garey A., Sabbagh, George J., Wenhin Chen, and Russell, Mark H.
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GROUNDWATER ,PESTICIDES ,LEACHING ,WATER quality ,PORE fluids ,ENVIRONMENTAL protection ,SOILS ,WATER - Abstract
The Root Zone Water Quality Model (RZWQM) and Pesticide Root Zone Model (PRZM) are currently being considered by the Office of Pesticide Programs (OPP) in the United States Environmental Protection Agency (US EPA) for Tier!! screening of pesticide leaching to groundwater (November 2005). The objective of the present research was to compare RZWQM and PRZM based on observed conservative tracer and pesticide pore water and soil concentrations collected in two unique groundwater leaching studies in North Carolina and Georgia. These two sites had been used previously by the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA) Environmental Model Validation Task Force (EMVTF) in the validation of PRZM. As in the FIFRA EMVTF PRZM validation, 'cold' modelling using input parameters based on EPA guidelines/databases and 'site-specific' modelling using field-measured soil and hydraulic parameters were performed with a recently released version of RZWQM called RZWQM-NAWQA (National Water Quality Assessment). Model calibration was not performed for either the 'cold' or 'site-specific' modelling. The models were compared based on predicted pore water and soil concentrations of bromide and pesticides throughout the soil profile. Both models tended to predict faster movement through the soil profile than observed. Based on a quantitative normalised objective function (NOF), RZWQM-NAWQA generally outperformed or was equivalent to PRZM in simulating pore water and soil concentrations. Both models were more successful in predicting soil concentrations (i.e. NOF < 1.0 for site-specific data, which satisfies site-specific applicability) than they were at predicting pore water concentrations. [ABSTRACT FROM AUTHOR]
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- 2006
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14. COMPARISON OF PESTICIDE ROOT ZONE MODEL 3.12: LEACHING PREDICTIONS WITH FIELD DATA.
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Russell, Mark H. and Jones, Russell L.
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PESTICIDES , *LEACHING - Abstract
Compares predictions of the pesticide root zone model (PRZM) 3.12 with measured data collected in nine different field leaching studies. Predictions of soil pore-water concentrations for pesticides for simulations based on the best choices for input parameters; Sensitivity of leaching to degradation rate.
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- 2002
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15. Sulfonylurea herbicides.
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Russell, Mark H., Saladini, John L., and Lichtner, Frank
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- 2002
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16. The use of pesticide leaching models in a regulatory setting: An industrial perspective.
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Russell, Mark H., Layton, Raymond J., and Tillotson, Patricia M.
- Abstract
Computer based simulation models are being used increasingly to predict the environmental fate of crop protection chemicals. Some considerations that should be given in selecting appropriate models for regulatory purposes include: model applicability, validation, capability, ease of use and documentation. Current applications of regulatory modeling include the rationalization of field data, evaluation of the leaching potential of pesticides and estimation of the probability of leaching. Problems commonly encountered in modeling include: limited accuracy, lack of defined objectives and standard modeling practices, and misuse of models and results. Models will continue to play an important role in the regulation of crop protection chemicals. It is important that regulators and industry agree on appropriate models and practices, and that regulatory decisions are not based solely on model results but take into account all available data. [ABSTRACT FROM PUBLISHER]
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- 1994
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17. Polyfluorinated chemicals in a spatially and temporally integrated food web in the Western Arctic
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Powley, Charles R., George, Stephen W., Russell, Mark H., Hoke, Robert A., and Buck, Robert C.
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SULFONATES , *ACIDS & the environment , *SPATIO-temporal variation , *ZOOPLANKTON , *BOREOGADUS saida , *SEALS (Animals) , *PHARMACOKINETICS - Abstract
This study reports on an investigation of the presence of polyfluorinated chemicals in a spatially and temporally integrated set of biological samples representing an Arctic food web. Zooplankton, Arctic cod, and seal tissues from the western Canadian Arctic were analyzed for perfluoroalkyl sulfonates [PFAS], perfluorocarboxylates [PFCAs], and other polyfluorinated acids. Perfluorooctane sulfonate [PFOS] was found in all samples [0.20–34ng/g] and in the highest concentrations. PFCAs from nine to 12 carbons were quantified in most of the samples [0.28–6.9ng/g]. PFCAs with carbon chain lengths of eight or less were not detected. Likewise, 8-2 fluorotelomer acid [8-2 FTA] and 8-2 fluorotelomer unsaturated acid [8-2 FTUA], products of fluorotelomer environmental transformation, were not detected. 2H,2H,3H,3H, heptadecafluoro decanoic acid [7-3 Acid], an additional metabolite from fluorotelomer biological transformation, was detected only in seal liver tissue [0.5–2.5ng/g]. The ratios of branched to linear PFOS isomers in fish and seal tissue were not similar and did not match that of technical PFOS as manufactured. No branched PFCA isomers were detected in any samples. It is concluded that differing pharmacokinetics complicate the use of branched to linear ratios of PFCAs in attributing their presence to a specific manufacturing process. A statistical analysis of the data revealed significant correlations between PFOS and the PFCAs detected as well as among the PFCAs themselves. The 7-3 Acid was not correlated with either PFCAs or PFAS, which suggests that it may have a different exposure pathway. [Copyright &y& Elsevier]
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- 2008
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18. Microbial transformation of 8:2 fluorotelomer acrylate and methacrylate in aerobic soils.
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Royer LA, Lee LS, Russell MH, Nies LF, and Turco RF
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- Acrylates chemistry, Aerobiosis, Alcohols chemistry, Biodegradation, Environmental, Biotransformation, Caprylates analysis, Caprylates chemistry, Carboxylic Acids analysis, Carboxylic Acids chemistry, Fluorocarbon Polymers, Fluorocarbons analysis, Fluorocarbons chemistry, Hydrocarbons, Fluorinated chemistry, Methacrylates chemistry, Models, Theoretical, Molecular Structure, Soil Pollutants chemistry, Acrylates analysis, Environmental Monitoring methods, Hydrocarbons, Fluorinated analysis, Methacrylates analysis, Soil Microbiology, Soil Pollutants analysis
- Abstract
Biotransformation of fluorotelomer (FT) compounds, such as 8:2 FT alcohol (FTOH) is now recognized to be a source of perfluorooctanoic acid (PFOA) as well as other perfluoroalkyl acids. In this study, microbially mediated hydrolysis of FT industrial intermediates 8:2 FT acrylate (8:2 FTAC) and 8:2 FT methacrylate (8:2 FTMAC) was evaluated in aerobic soils for up to 105d. At designated times, triplicate microcosms were sacrificed by sampling the headspace for volatile FTOHs followed by sequential extraction of soil for the parent monomers as well as transient and terminal degradation products. Both FTAC and FTMAC were hydrolyzed at the ester linkage as evidenced by 8:2 FTOH production. 8:2 FTAC and FTMAC degraded rapidly with half-lives ⩽5d and 15d, respectively. Maximum 8:2 FTOH levels were 6-13mol% within 3-6d. Consistent with the known biotransformation pathway of 8:2 FTOH, FT carboxylic acids and perfluoroalkyl carboxylic acids were subsequently generated including up to 10.3mol% of PFOA (105d). A total mass balance (parent plus metabolites) of 50-75mol% was observed on the last sampling day. 7:2 sFTOH, a direct precursor to PFOA, unexpectedly increased throughout the incubation period. The likely, but unconfirmed, concomitant production of acrylic acids was proposed as altering expected degradation patterns. Biotransformation of 8:2 FTAC, 8:2 FTMAC, and previously reported 8:2 FT-stearate for the same soils revealed the effect of the non-fluorinated terminus group linked to the FT chain on the electronic differences that affect microbially-mediated ester cleavage rates., (Copyright © 2014 Elsevier Ltd. All rights reserved.)
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- 2015
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19. Calculation of chemical elimination half-life from blood with an ongoing exposure source: the example of perfluorooctanoic acid (PFOA).
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Russell MH, Waterland RL, and Wong F
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- Adult, Cross-Sectional Studies, Environmental Monitoring, Half-Life, Humans, Caprylates pharmacokinetics, Fluorocarbons pharmacokinetics
- Abstract
Determination of the chemical clearance rate from human blood is a critical component of toxicokinetic exposure assessment. Analysis of temporal biomonitoring data without consideration of ongoing exposure results in calculation of apparent elimination half-life values that are longer than the intrinsic value. The intrinsic elimination half-life is solely a function of the rate of elimination while the apparent elimination half-life reflects the processes of both elimination and ongoing exposure. Confusion between intrinsic and apparent half-life values can lead to misinterpretation of biomonitoring data and can result in exaggerated predictions in subsequent modeling efforts. This work provides a review of the first-order equations that have been developed to calculate intrinsic and apparent half-life values and the potential bias that can result from confusing these two values. Published human biomonitoring data for perfluorooctanoic acid (PFOA) are analyzed using these equations to provide examples of low, medium and high bias in determination of the intrinsic elimination half-life from plasma or serum, the components of blood typically analyzed for PFOA. An approach is also provided to estimate the extent of exposure reduction that is indicated by declining longitudinal or cross-sectional biomonitoring data. Based on the evaluation methodology presented in this work, the intrinsic elimination half-life of PFOA in humans is 2.4years, representing the average of independent estimates of 2.5years (95% CI, 2.4-2.7) and 2.3years (95% CI, 2.1-2.4). The declining concentration of PFOA in blood of the general USA adult population represents an estimated exposure reduction of 20-30% over the period 1999-2008., (Copyright © 2014 Elsevier Ltd. All rights reserved.)
- Published
- 2015
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20. Renal elimination of perfluorocarboxylates (PFCAs).
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Han X, Nabb DL, Russell MH, Kennedy GL, and Rickard RW
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- Animals, Humans, Models, Biological, Caprylates pharmacokinetics, Carboxylic Acids pharmacokinetics, Environmental Pollutants pharmacokinetics, Fluorocarbons pharmacokinetics, Kidney metabolism
- Abstract
Sex-, species-, and chain length-dependent renal elimination is the hallmark of mammalian elimination of perfluorocarboxylates (PFCAs) and has been extensively studied for almost 30 years. In this review, toxicokinetic data of PFCAs (chain lengths ranging from 4 to 10) in different species are compared with an emphasis on their relevance to renal elimination. PFCAs vary in their affinities to bind to serum albumins in plasma, which is an important factor in determining the renal clearance of PFCAs. PFCA-albumin binding has been well characterized and is summarized in this review. The mechanism of the sex-, species-, and chain length-dependent renal PFCA elimination is a research area that has gained continuous interest since the beginning of toxicological studies of PFCAs. It is now recognized that organic anion transport proteins play a key role in PFCA renal tubular reabsorption, a process that is sex-, species-, and chain length-dependent. Recent studies on the identification of PFCA renal transport proteins and characterization of their transport kinetics have greatly improved our understanding of the PFCA renal transport mechanism at the molecular level. A mathematical representation of this renal tubular reabsorption mechanism has been incorporated in physiologically based pharmacokinetic (PBPK) modeling of perfluorooctanoate (PFOA). Improvement of PBPK models in the future will require more accurate and quantitative characterization of renal transport pathways of PFCAs. To that end, a basolateral membrane efflux pathway for the reabsorption of PFCAs in the kidney is discussed in this review, which could provide a future research direction toward a better understanding of the mechanisms of PFCA renal elimination.
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- 2012
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21. Comment on "Degradability of an acrylate-linked, fluorotelomer polymer in soil".
- Author
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Russell MH, Wang N, Berti WR, Szostek B, and Buck RC
- Subjects
- Fluorocarbon Polymers analysis, Fluorocarbon Polymers chemistry, Fluorocarbons analysis, Gas Chromatography-Mass Spectrometry, Models, Theoretical, Acrylates chemistry, Environmental Restoration and Remediation, Hydrocarbons, Fluorinated chemistry, Soil Pollutants chemistry
- Published
- 2010
- Full Text
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22. Partitioning and removal of perfluorooctanoate during rain events: the importance of physical-chemical properties.
- Author
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Barton CA, Kaiser MA, and Russell MH
- Subjects
- Air Pollutants analysis, Caprylates analysis, Environmental Monitoring, Fluorocarbons analysis, Hydrogen-Ion Concentration, Ions, Kinetics, Particle Size, Rain, Volatilization, Air Pollutants chemistry, Caprylates chemistry, Fluorocarbons chemistry
- Abstract
The potential for airborne emissions to undergo long-range transport or to be removed from the atmosphere is influenced by their physical-chemical properties. When perfluorooctanate (PFO) enters the environment, its physical-chemical properties can vary significantly, depending on whether it exists as an acid, a salt, or a dissociated ion. A summary of the physical-chemical properties of the three most likely environmental states: ammonium perfluorooctanoate (APFO), perfluorooctanoic acid (PFOA) and the dissociated perfluorooctanoate anion (PFO(-)) is presented to illustrate the distinct environmental properties of each. The most volatile species, PFOA, is shown to have a pH-dependent air-water partitioning coefficient (K(aw)). The variability of K(aw) with pH influences the potential for vapor formation from aqueous environments, including rain events. Using the pH-dependent K(aw) and measured rain and air concentrations, it is shown that vapor-phase PFOA is not likely to be present above measurable levels of 0.2 ng m(-3) (12 parts per quadrillion v/v) during a rain event. Because rain concentrations determined in this work are comparable to measurements in other parts of North America, it is unlikely that rain events are a significant source of vapor-phase PFOA for the general North American region. It is shown that PFOA exists primarily in the particle phase in ambient air near direct sources of emissions and is efficiently scavenged by rain droplets, making wet deposition an important removal mechanism for emissions originating as either PFOA or APFO. Washout ratios of particle-associated PFO were determined to range between 1 x 10(5) and 5 x 10(5), in the same range as other semi-volatile compounds for which wet deposition is an important mechanism for atmospheric removal and deposition onto soils and water bodies.
- Published
- 2007
- Full Text
- View/download PDF
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