Atmospheric fate of poly- and perfluorinated alkyl substances (PFASs): II. Emission source strength in summer in Zurich, Switzerland

Publikation: Beiträge in ZeitschriftenZeitschriftenaufsätzeForschungbegutachtet

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Atmospheric fate of poly- and perfluorinated alkyl substances (PFASs): II. Emission source strength in summer in Zurich, Switzerland. / Wang, Zhanyun; Scheringer, Martin; MacLeod, Matthew et al.
in: Environmental Pollution, Jahrgang 169, 10.2012, S. 204-209.

Publikation: Beiträge in ZeitschriftenZeitschriftenaufsätzeForschungbegutachtet

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Wang Z, Scheringer M, MacLeod M, Bogdal C, Müller C, Gerecke A et al. Atmospheric fate of poly- and perfluorinated alkyl substances (PFASs): II. Emission source strength in summer in Zurich, Switzerland. Environmental Pollution. 2012 Okt;169:204-209. doi: 10.1016/j.envpol.2012.03.037

Bibtex

@article{c5e3aea9c74f4eb1a6332e7c6a6e62d5,
title = "Atmospheric fate of poly- and perfluorinated alkyl substances (PFASs): II. Emission source strength in summer in Zurich, Switzerland",
abstract = "Fluorotelomer alcohols (FTOHs) and perfluorooctane sulfonamides (FOSAs) are present in consumer products and are semi-volatile precursors of persistent perfluoroalkyl acids (PFAAs). The high variability of levels of FTOHs and FOSAs in products makes it difficult to derive FTOH- and FOSA-emissions from urban areas based on emission factors. Here we used a multimedia mass balance model that describes the day–night cycle of semi-volatile organic chemicals in air to interpret measurements of 8:2 FTOH, 10:2 FTOH, MeFOSA and EtFOSA from a sampling campaign in summer 2010 in Zurich, Switzerland. The estimated emission source strength of the four substances follows the sequence: 8:2 FTOH (2.6 g/h) > 10:2 FTOH (0.75 g/h) > MeFOSA (0.08 g/h) > EtFOSA (0.05 g/h). There is no FTOHs- or FOSAs-related industry in Zurich. Accordingly, our estimates are representative of diffusive emissions during use and disposal of consumer products, and describe noticeable sources of these PFASs to the environment.",
keywords = "Chemistry, Fluorotelomer alcohols, FTOHs, Perfluorooctane sulfonamides, FOSAs, Emission source strength, Nocturnal boundary layer, Diel pattern",
author = "Zhanyun Wang and Martin Scheringer and Matthew MacLeod and Christian Bogdal and Claudia M{\"u}ller and Andreas Gerecke and Konrad Hungerbuehler",
year = "2012",
month = oct,
doi = "10.1016/j.envpol.2012.03.037",
language = "English",
volume = "169",
pages = "204--209",
journal = "Environmental Pollution",
issn = "0269-7491",
publisher = "Elsevier B.V.",

}

RIS

TY - JOUR

T1 - Atmospheric fate of poly- and perfluorinated alkyl substances (PFASs)

T2 - II. Emission source strength in summer in Zurich, Switzerland

AU - Wang, Zhanyun

AU - Scheringer, Martin

AU - MacLeod, Matthew

AU - Bogdal, Christian

AU - Müller, Claudia

AU - Gerecke, Andreas

AU - Hungerbuehler, Konrad

PY - 2012/10

Y1 - 2012/10

N2 - Fluorotelomer alcohols (FTOHs) and perfluorooctane sulfonamides (FOSAs) are present in consumer products and are semi-volatile precursors of persistent perfluoroalkyl acids (PFAAs). The high variability of levels of FTOHs and FOSAs in products makes it difficult to derive FTOH- and FOSA-emissions from urban areas based on emission factors. Here we used a multimedia mass balance model that describes the day–night cycle of semi-volatile organic chemicals in air to interpret measurements of 8:2 FTOH, 10:2 FTOH, MeFOSA and EtFOSA from a sampling campaign in summer 2010 in Zurich, Switzerland. The estimated emission source strength of the four substances follows the sequence: 8:2 FTOH (2.6 g/h) > 10:2 FTOH (0.75 g/h) > MeFOSA (0.08 g/h) > EtFOSA (0.05 g/h). There is no FTOHs- or FOSAs-related industry in Zurich. Accordingly, our estimates are representative of diffusive emissions during use and disposal of consumer products, and describe noticeable sources of these PFASs to the environment.

AB - Fluorotelomer alcohols (FTOHs) and perfluorooctane sulfonamides (FOSAs) are present in consumer products and are semi-volatile precursors of persistent perfluoroalkyl acids (PFAAs). The high variability of levels of FTOHs and FOSAs in products makes it difficult to derive FTOH- and FOSA-emissions from urban areas based on emission factors. Here we used a multimedia mass balance model that describes the day–night cycle of semi-volatile organic chemicals in air to interpret measurements of 8:2 FTOH, 10:2 FTOH, MeFOSA and EtFOSA from a sampling campaign in summer 2010 in Zurich, Switzerland. The estimated emission source strength of the four substances follows the sequence: 8:2 FTOH (2.6 g/h) > 10:2 FTOH (0.75 g/h) > MeFOSA (0.08 g/h) > EtFOSA (0.05 g/h). There is no FTOHs- or FOSAs-related industry in Zurich. Accordingly, our estimates are representative of diffusive emissions during use and disposal of consumer products, and describe noticeable sources of these PFASs to the environment.

KW - Chemistry

KW - Fluorotelomer alcohols

KW - FTOHs

KW - Perfluorooctane sulfonamides

KW - FOSAs

KW - Emission source strength

KW - Nocturnal boundary layer

KW - Diel pattern

UR - http://www.scopus.com/inward/record.url?scp=84863793574&partnerID=8YFLogxK

U2 - 10.1016/j.envpol.2012.03.037

DO - 10.1016/j.envpol.2012.03.037

M3 - Journal articles

C2 - 22621939

VL - 169

SP - 204

EP - 209

JO - Environmental Pollution

JF - Environmental Pollution

SN - 0269-7491

ER -

DOI