Journal cover Journal topic
Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
Atmos. Chem. Phys., 11, 7027-7044, 2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.
Research article
20 Jul 2011
Quantification of aerosol chemical composition using continuous single particle measurements
C.-H. Jeong1, M. L. McGuire1, K. J. Godri2, J. G. Slowik1,*, P. J. G. Rehbein1, and G. J. Evans1 1Southern Ontario Centre for Atmospheric Aerosol Research, University of Toronto, 200 College Street, Toronto, Ontario, M5S 3E5, Canada
2Division of Environmental Health & Risk Management, School of Geography, Earth & Environmental Sciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK
*now at: Paul Scherrer Institute, 5232 Villigen PSI, Switzerland
Abstract. Mass concentrations of sulphate, nitrate, ammonium, organic carbon (OC), elemental carbon (EC) were determined from real time single particle data in the size range 0.1–3.0 μm measured by an Aerosol Time-of-Flight Mass Spectrometer (ATOFMS) at urban and rural sites in Canada. To quantify chemical species within individual particles measured by an ATOFMS, ion peak intensity of m/z −97 for sulphate, −62 for nitrate, +18 for ammonium, +43 for OC, and +36 for EC were scaled using the number and size distribution data by an Aerodynamic Particle Sizer (APS) and a Fast Mobility Particle Sizer (FMPS). Hourly quantified chemical species from ATOFMS single-particle analysis were compared with collocated fine particulate matter (aerodynamic diameter < 2.5 μm, PM2.5) chemical composition measurements by an Aerosol Mass Spectrometer (AMS) at a rural site, a Gas-Particle Ion Chromatograph (GPIC) at an urban site, and a Sunset Lab field OCEC analyzer at both sites. The highest correlation was found for nitrate, with correlation coefficients (Pearson r) of 0.89 (ATOFMS vs. GPIC) and 0.85 (ATOFMS vs. AMS). ATOFMS mass calibration factors, determined for the urban site, were used to calculate mass concentrations of the major PM2.5 chemical components at the rural site near the US border in southern Ontario. Mass reconstruction using the ATOFMS mass calibration factors agreed very well with the PM2.5 mass concentrations measured by a Tapered Element Oscillating Microbalance (TEOM, r = 0.86) at the urban site and a light scattering monitor (DustTrak, r = 0.87) at the rural site. In the urban area nitrate was the largest contributor to PM2.5 mass in the winter, while organics and sulphate contributed ~64 % of the summer PM2.5 in the rural area, suggesting a strong influence of regional/trans-boundary pollution. The mass concentrations of five major species in ten size-resolved particle-types and aerosol acidity of each particle-type were determined for the rural site. On a mass basis sulphate and OC rich particle-types (OC-S and OC-S-N) accounted for up to 59 % of the particles characterized and aerosols were weakly acidic in the rural area. This is the first study to estimate hourly quantitative data of sulphate, nitrate, ammonium, OC and EC in ambient particles from scaled ATOFMS single particle analysis; these were closely comparable with collocated high time resolution data of sulphate, nitrate and ammonium detected by AMS and GPIC.

Citation: Jeong, C.-H., McGuire, M. L., Godri, K. J., Slowik, J. G., Rehbein, P. J. G., and Evans, G. J.: Quantification of aerosol chemical composition using continuous single particle measurements, Atmos. Chem. Phys., 11, 7027-7044,, 2011.
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