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Atmospheric transport of PCDD/Fs in air masses across the UK and Ireland: evidence of emissions and depletion.

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Atmospheric transport of PCDD/Fs in air masses across the UK and Ireland: evidence of emissions and depletion. / Lohmann, Rainer; Green, Nicholas J. L.; Jones, Kevin C.
In: Environmental Science and Technology, Vol. 33, No. 17, 01.09.1999, p. 2872-2878.

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Lohmann R, Green NJL, Jones KC. Atmospheric transport of PCDD/Fs in air masses across the UK and Ireland: evidence of emissions and depletion. Environmental Science and Technology. 1999 Sept 1;33(17):2872-2878. doi: 10.1021/es981011j

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Lohmann, Rainer ; Green, Nicholas J. L. ; Jones, Kevin C. / Atmospheric transport of PCDD/Fs in air masses across the UK and Ireland: evidence of emissions and depletion. In: Environmental Science and Technology. 1999 ; Vol. 33, No. 17. pp. 2872-2878.

Bibtex

@article{53f1a1a239094515b9d284999951fdbd,
title = "Atmospheric transport of PCDD/Fs in air masses across the UK and Ireland: evidence of emissions and depletion.",
abstract = "A sample extraction/cleanup and high-resolution gas chromatography−high-resolution mass spectrometry procedure is described and used to routinely quantify the full range of 2,3,7,8-substituted polychlorinated dibenzo-p-dioxanes and dibenzofurans (PCDD/Fs) and di- to octa-homologue groups in samples of 500−1000 m3 of remote/rural European air. The relative standard deviations of sum of toxic equivalents (ΣTEQ) and ΣPCDD/F concentrations from five concurrent samples each of 700 m3 air were 10 and 11%, respectively. Air samples for PCDD/Fs were taken simultaneously at three sites in May 1997: (i) on the remote western Irish coast, (ii) on the northwest coast of England, and (iii) at a regional background site in the northeast of England. For three sampling events where the air passed successively over the two English sites, the increase in air concentrations was used to calculate an emission rate for the mainland United Kingdom land mass; this crude approach gave values of 2−12 g ΣTEQ/day, which is broadly in line with annual primary atmospheric source inventory estimates. For another event, when an air mass moved successively over the north of England to the Irish west coast, atmospheric half-lives were calculated to be 0.3−4 days for different homologues, which is broadly in line with laboratory and theoretical estimates.",
author = "Rainer Lohmann and Green, {Nicholas J. L.} and Jones, {Kevin C.}",
year = "1999",
month = sep,
day = "1",
doi = "10.1021/es981011j",
language = "English",
volume = "33",
pages = "2872--2878",
journal = "Environmental Science and Technology",
issn = "0013-936X",
publisher = "American Chemical Society",
number = "17",

}

RIS

TY - JOUR

T1 - Atmospheric transport of PCDD/Fs in air masses across the UK and Ireland: evidence of emissions and depletion.

AU - Lohmann, Rainer

AU - Green, Nicholas J. L.

AU - Jones, Kevin C.

PY - 1999/9/1

Y1 - 1999/9/1

N2 - A sample extraction/cleanup and high-resolution gas chromatography−high-resolution mass spectrometry procedure is described and used to routinely quantify the full range of 2,3,7,8-substituted polychlorinated dibenzo-p-dioxanes and dibenzofurans (PCDD/Fs) and di- to octa-homologue groups in samples of 500−1000 m3 of remote/rural European air. The relative standard deviations of sum of toxic equivalents (ΣTEQ) and ΣPCDD/F concentrations from five concurrent samples each of 700 m3 air were 10 and 11%, respectively. Air samples for PCDD/Fs were taken simultaneously at three sites in May 1997: (i) on the remote western Irish coast, (ii) on the northwest coast of England, and (iii) at a regional background site in the northeast of England. For three sampling events where the air passed successively over the two English sites, the increase in air concentrations was used to calculate an emission rate for the mainland United Kingdom land mass; this crude approach gave values of 2−12 g ΣTEQ/day, which is broadly in line with annual primary atmospheric source inventory estimates. For another event, when an air mass moved successively over the north of England to the Irish west coast, atmospheric half-lives were calculated to be 0.3−4 days for different homologues, which is broadly in line with laboratory and theoretical estimates.

AB - A sample extraction/cleanup and high-resolution gas chromatography−high-resolution mass spectrometry procedure is described and used to routinely quantify the full range of 2,3,7,8-substituted polychlorinated dibenzo-p-dioxanes and dibenzofurans (PCDD/Fs) and di- to octa-homologue groups in samples of 500−1000 m3 of remote/rural European air. The relative standard deviations of sum of toxic equivalents (ΣTEQ) and ΣPCDD/F concentrations from five concurrent samples each of 700 m3 air were 10 and 11%, respectively. Air samples for PCDD/Fs were taken simultaneously at three sites in May 1997: (i) on the remote western Irish coast, (ii) on the northwest coast of England, and (iii) at a regional background site in the northeast of England. For three sampling events where the air passed successively over the two English sites, the increase in air concentrations was used to calculate an emission rate for the mainland United Kingdom land mass; this crude approach gave values of 2−12 g ΣTEQ/day, which is broadly in line with annual primary atmospheric source inventory estimates. For another event, when an air mass moved successively over the north of England to the Irish west coast, atmospheric half-lives were calculated to be 0.3−4 days for different homologues, which is broadly in line with laboratory and theoretical estimates.

U2 - 10.1021/es981011j

DO - 10.1021/es981011j

M3 - Journal article

VL - 33

SP - 2872

EP - 2878

JO - Environmental Science and Technology

JF - Environmental Science and Technology

SN - 0013-936X

IS - 17

ER -