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

Author:

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

Abstract

Abstract. 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. 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−3 (on average 1.5 μg m−3). 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 (r = 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.

Publisher

Copernicus GmbH

Subject

Atmospheric Science

Reference59 articles.

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