Atmospheric Measurement Techniques (Aug 2010)

High time-resolution chemical characterization of the water-soluble fraction of ambient aerosols with PILS-TOC-IC and AMS

  • H. Timonen,
  • M. Aurela,
  • S. Carbone,
  • K. Saarnio,
  • S. Saarikoski,
  • T. Mäkelä,
  • M. Kulmala,
  • V.-M. Kerminen,
  • D. R. Worsnop,
  • R. Hillamo

DOI
https://doi.org/10.5194/amt-3-1063-2010
Journal volume & issue
Vol. 3, no. 4
pp. 1063 – 1074

Abstract

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A particle-into-liquid sampler (PILS) was coupled with a total organic carbon analyzer (TOC) and two ion chromatographs (IC) to enable high time-resolution measurements of water-soluble ions and water-soluble organic carbon (WSOC) by a single sampling and analytical set-up. The new high time-resolution measurement system, the PILS-TOC-IC, was able to provide essential chemical and physical information about fast changes in composition, concentrations and likely sources of the water-soluble fraction of atmospheric aerosol. The concentrations of major water-soluble ions and WSOC were measured by the PILS-TOC-IC system from 25 April to 28 May 2009. <br><br> The data of the PILS-TOC-IC setup was compared with the data from the High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) data measured from 25 April to 8 May 2009. The measured water-soluble particulate organic matter (WSPOM) concentration varied typically from 0.10 to 8.8 μg m<sup>−3</sup> (on average 1.5 μg m<sup>−3</sup>). The WSPOM contributed on average 51% to particulate organic matter (POM) measured with the AMS. The correlation between the data of all the online measurement devices (AMS, PILS-TOC-IC, semicontinuous EC/OC carbon analyzer and TEOM) was excellent. For sulfate, nitrate and ammonium the correlations between the PILS-TOC-IC and AMS were 0.93, 0.96 and 0.96, respectively. The correlation between WSPOM and POM was also strong (<I>r</I> = 0.88). The identified sources of WSPOM were long-range transported biomass burning and secondary organic aerosol (SOA) formation. WSPOM and oxalate produced in biomass burning were clearly correlated with carbon monoxide.