Heated submicron particle fluxes using an optical particle counter in urban environment

From May 2008 to March 2009 aerosol emissions were measured using the eddy covariance method covering the size range 0.25 to 2.5 μm diameter (<i>D</i><sub>p</sub>) from a 105 m tower, in central Stockholm, Sweden. Supporting chemical aerosol data were collected at roof and st...

Full description

Bibliographic Details
Main Authors: M. Vogt, C. Johansson, M. Mårtensson, H. Struthers, L. Ahlm, D. Nilsson
Format: Article
Language:English
Published: Copernicus Publications 2013-03-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/13/3087/2013/acp-13-3087-2013.pdf
id doaj-ada9bd966af24cff903f938f1816d1d3
record_format Article
spelling doaj-ada9bd966af24cff903f938f1816d1d32020-11-24T23:21:10ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242013-03-011363087309610.5194/acp-13-3087-2013Heated submicron particle fluxes using an optical particle counter in urban environmentM. VogtC. JohanssonM. MårtenssonH. StruthersL. AhlmD. NilssonFrom May 2008 to March 2009 aerosol emissions were measured using the eddy covariance method covering the size range 0.25 to 2.5 μm diameter (<i>D</i><sub>p</sub>) from a 105 m tower, in central Stockholm, Sweden. Supporting chemical aerosol data were collected at roof and street level. Results show that the inorganic fraction of sulfate, nitrate, ammonium and sea salt accounts for approximately 15% of the total aerosol mass < 1 μm <i>D</i><sub>p</sub> (PM<sub>1</sub>) with water soluble soil contributing 11% and water insoluble soil 47%. Carbonaceous compounds were at the most 27% of PM<sub>1</sub> mass. It was found that heating the air from the tower to 200 &deg;C resulted in the loss of approximately 60% of the aerosol volume at 0.25 μm <i>D</i><sub>p</sub> whereas only 40% of the aerosol volume was removed at 0.6 μm <i>D</i><sub>p</sub>. Further heating to 300 &deg;C caused very little additional losses <0.6 μm <i>D</i><sub>p</sub>. The chemical analysis did not include carbonaceous compounds, but based on the difference between the total mass concentration and the sum of the analyzed non-carbonaceous materials, it can be assumed that the non-volatile particulate material (heated to 300 &deg;C) consists mainly of carbonaceous compounds, including elemental carbon. Furthermore, it was found that the non-volatile particle fraction <0.6 μm <i>D</i><sub>p</sub> correlated (<i>r</i><sup>2</sup> = 0.4) with the BC concentration at roof level in the city, supporting the assumption that the non-volatile material consists of carbonaceous compounds. The average diurnal cycles of the BC emissions from road traffic (as inferred from the ratio of the incremental concentrations of nitrogen oxides (NO<sub>x</sub>) and BC measured on a densely trafficked street) and the fluxes of non-volatile material at tower level are in close agreement, suggesting a traffic source of BC. We have estimated the emission factors (EFs) for non-volatile particles <0.6 μm <i>D</i><sub>p</sub> to be 2.4 &plusmn; 1.4 mg veh<sup>&minus;1</sup> km<sup>&minus;1</sup> based on either CO<sub>2</sub> fluxes or traffic activity data. Light (LDV) and heavy duty vehicle (HDV) EFs were estimated using multiple linear regression and reveal that for non-volatile particulate matter in the 0.25 to 0.6 μm <i>D</i><sub>p</sub> range, the EF<sub>HDV</sub> is approximately twice as high as the EF<sub>LDV</sub>, the difference not being statistically significant.http://www.atmos-chem-phys.net/13/3087/2013/acp-13-3087-2013.pdf
collection DOAJ
language English
format Article
sources DOAJ
author M. Vogt
C. Johansson
M. Mårtensson
H. Struthers
L. Ahlm
D. Nilsson
spellingShingle M. Vogt
C. Johansson
M. Mårtensson
H. Struthers
L. Ahlm
D. Nilsson
Heated submicron particle fluxes using an optical particle counter in urban environment
Atmospheric Chemistry and Physics
author_facet M. Vogt
C. Johansson
M. Mårtensson
H. Struthers
L. Ahlm
D. Nilsson
author_sort M. Vogt
title Heated submicron particle fluxes using an optical particle counter in urban environment
title_short Heated submicron particle fluxes using an optical particle counter in urban environment
title_full Heated submicron particle fluxes using an optical particle counter in urban environment
title_fullStr Heated submicron particle fluxes using an optical particle counter in urban environment
title_full_unstemmed Heated submicron particle fluxes using an optical particle counter in urban environment
title_sort heated submicron particle fluxes using an optical particle counter in urban environment
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2013-03-01
description From May 2008 to March 2009 aerosol emissions were measured using the eddy covariance method covering the size range 0.25 to 2.5 μm diameter (<i>D</i><sub>p</sub>) from a 105 m tower, in central Stockholm, Sweden. Supporting chemical aerosol data were collected at roof and street level. Results show that the inorganic fraction of sulfate, nitrate, ammonium and sea salt accounts for approximately 15% of the total aerosol mass < 1 μm <i>D</i><sub>p</sub> (PM<sub>1</sub>) with water soluble soil contributing 11% and water insoluble soil 47%. Carbonaceous compounds were at the most 27% of PM<sub>1</sub> mass. It was found that heating the air from the tower to 200 &deg;C resulted in the loss of approximately 60% of the aerosol volume at 0.25 μm <i>D</i><sub>p</sub> whereas only 40% of the aerosol volume was removed at 0.6 μm <i>D</i><sub>p</sub>. Further heating to 300 &deg;C caused very little additional losses <0.6 μm <i>D</i><sub>p</sub>. The chemical analysis did not include carbonaceous compounds, but based on the difference between the total mass concentration and the sum of the analyzed non-carbonaceous materials, it can be assumed that the non-volatile particulate material (heated to 300 &deg;C) consists mainly of carbonaceous compounds, including elemental carbon. Furthermore, it was found that the non-volatile particle fraction <0.6 μm <i>D</i><sub>p</sub> correlated (<i>r</i><sup>2</sup> = 0.4) with the BC concentration at roof level in the city, supporting the assumption that the non-volatile material consists of carbonaceous compounds. The average diurnal cycles of the BC emissions from road traffic (as inferred from the ratio of the incremental concentrations of nitrogen oxides (NO<sub>x</sub>) and BC measured on a densely trafficked street) and the fluxes of non-volatile material at tower level are in close agreement, suggesting a traffic source of BC. We have estimated the emission factors (EFs) for non-volatile particles <0.6 μm <i>D</i><sub>p</sub> to be 2.4 &plusmn; 1.4 mg veh<sup>&minus;1</sup> km<sup>&minus;1</sup> based on either CO<sub>2</sub> fluxes or traffic activity data. Light (LDV) and heavy duty vehicle (HDV) EFs were estimated using multiple linear regression and reveal that for non-volatile particulate matter in the 0.25 to 0.6 μm <i>D</i><sub>p</sub> range, the EF<sub>HDV</sub> is approximately twice as high as the EF<sub>LDV</sub>, the difference not being statistically significant.
url http://www.atmos-chem-phys.net/13/3087/2013/acp-13-3087-2013.pdf
work_keys_str_mv AT mvogt heatedsubmicronparticlefluxesusinganopticalparticlecounterinurbanenvironment
AT cjohansson heatedsubmicronparticlefluxesusinganopticalparticlecounterinurbanenvironment
AT mmartensson heatedsubmicronparticlefluxesusinganopticalparticlecounterinurbanenvironment
AT hstruthers heatedsubmicronparticlefluxesusinganopticalparticlecounterinurbanenvironment
AT lahlm heatedsubmicronparticlefluxesusinganopticalparticlecounterinurbanenvironment
AT dnilsson heatedsubmicronparticlefluxesusinganopticalparticlecounterinurbanenvironment
_version_ 1725572461271973888