Characterizing the Air Emissions, Transport, and Deposition of Per- and Polyfluoroalkyl Substances from a Fluoropolymer Manufacturing Facility

被引:89
作者
D'Ambro, Emma L. [1 ,4 ]
Pye, Havala O. T. [1 ]
Bash, Jesse O. [1 ]
Bowyer, James [2 ]
Allen, Chris [3 ]
Efstathiou, Christos [3 ]
Gilliam, Robert C. [1 ]
Reynolds, Lara [3 ]
Talgo, Kevin [3 ]
Murphy, Benjamin N. [1 ]
机构
[1] US EPA, Ctr Environm Measurement & Modeling, Res Triangle Pk, NC 27711 USA
[2] NC DEQ, North Carolina Div Air Qual, Raleigh, NC 27603 USA
[3] Gen Dynam Informat Technol, Res Triangle Pk, NC 28311 USA
[4] Oak Ridge Inst Sci Educ, Oak Ridge, TN 37831 USA
关键词
DRINKING-WATER CONTAMINANTS; CAPE FEAR RIVER; PERFLUORINATED COMPOUNDS; POLYFLUORINATED COMPOUNDS; TRIFLUOROACETIC-ACID; MASS-SPECTROMETRY; ORGANIC-COMPOUNDS; ALKYL SUBSTANCES; PERFLUOROALKYL; PERFLUOROOCTANOATE;
D O I
10.1021/acs.est.0c06580
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Per- and polyfluoroalkyl substances (PFASs) have been released into the environment for decades, yet contributions of air emissions to total human exposure, from inhalation and drinking water contamination via deposition, are poorly constrained. The atmospheric transport and fate of a PFAS mixture from a fluoropolymer manufacturing facility in North Carolina were investigated with the Community Multiscale Air Quality (CMAQ) model applied at high resolution (1 km) and extending similar to 150 km from the facility. Twenty-six explicit PFAS compounds, including GenX, were added to CMAQ using current best estimates of air emissions and relevant physicochemical properties. The new model, CMAQ-PFAS, predicts that 5% by mass of total emitted PFAS and 2.5% of total GenX are deposited within similar to 150 km of the facility, with the remainder transported out. Modeled air concentrations of total GenX and total PFAS around the facility can reach 24.6 and 8500 ng m(-3) but decrease to similar to 0.1 and similar to 10 ng m(-3) at 35 km downwind, respectively. We find that compounds with acid functionality have higher deposition due to enhanced water solubility and pH-driven partitioning to aqueous media. To our knowledge, this is the first modeling study of the fate of a comprehensive, chemically resolved suite of PFAS air emissions from a major manufacturing source.
引用
收藏
页码:862 / 870
页数:9
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