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Airborne measurement of inorganic ionic components of fine aerosol particles using the particle‐into‐liquid sampler coupled to ion chromatography technique during ACE‐Asia and TRACE‐P
Journal article   Open access   Peer reviewed

Airborne measurement of inorganic ionic components of fine aerosol particles using the particle‐into‐liquid sampler coupled to ion chromatography technique during ACE‐Asia and TRACE‐P

Y.‐N. Lee, R. Weber, Y. Ma, D. Orsini, K. Maxwell‐Meier, D. Blake, S. Meinardi, G. Sachse, C. Harward, T.‐Y. Chen, …
Journal of Geophysical Research: Atmospheres, v 108(D23), pp 8646-n/a
16 Dec 2003
url
https://doi.org/10.1029/2002jd003265View
Published, Version of Record (VoR) Open Maybe Open Access (Publisher Bronze)
url
https://doi.org/10.1029/2002JD003265View
Published, Version of Record (VoR) Open

Abstract

ACE‐Asia Aerosol Composition PILS TRACE‐P
Eight inorganic ions in fine aerosol particles (Dp < 1.3 μm) were measured on board the NCAR C130 and NASA P‐3B aircraft during the 2001 Aerosol Characterization Experiment (ACE)‐Asia and the Transport and Chemical Evolution over the Pacific (TRACE‐P) experiments, respectively. Concentrations of NH4+, SO42−, NO3−, Ca2+, K+, Mg2+, Na+, and Cl− were determined using a particle‐into‐liquid sampler coupled to ion chromatography (PILS‐IC) technique at a 4‐min resolution and a limit of detection <0.05 μg m−3. The maximum total ion concentrations observed on the C130 and the P‐3B were 27 μg m−3 and 84 μg m−3, respectively. During ACE‐Asia, NH4+ and SO42− dominated, with the dust‐derived Ca2+ contributing nearly equally as SO42− in mixing ratios. The sea‐salt‐derived Na+ and Cl− were comparable to biomass‐burning tracer K+, showing >1 ppbv only in the top 1% sample population. During TRACE‐P, NH4+ dominated, followed by SO42−, Cl−, Na+, NO3−, Ca2+, and K+, in decreasing order of importance. In addition to a sea‐salt origin, Cl− showed a source in urban emissions possibly related to biofuel combustion. Both sea salt and dust contributed to Mg2+. In both experiments, NH4+, SO42−, NO3−, and CO were strongly correlated, indicating that combustion was the dominant source of these species and that NH3 and other alkaline materials were in sufficient supply to neutralize H2SO4. The [NH4+] to ([NO3−] + 2[SO42−]) ratio was ∼0.70 in the two campaigns, with deviations found only in volcano plumes, whereby SO42− was found to correlate with SO2. Charge balance of the ions showed both positive and negative deviations whose magnitudes, ∼30%, provide estimates of the lower limits of unmeasured ions. Elevated NO3− and Ca2+ coexist mainly under polluted conditions, suggesting the importance of sequestering HNO3 by mineral dust.

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Meteorology & Atmospheric Sciences
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