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JOURNAL OF GEOPHYSICAL RESEARCH,
VOL. 108, NO. D23,
8646,
doi:10.1029/2002JD003265,
2003
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
Atmospheric Sciences Division, Brookhaven National Laboratory, Upton, New York, USA
R. Weber
School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA
Y. Ma
School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA
D. Orsini
School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA
K. Maxwell-Meier
School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA
D. Blake
Department of Chemistry, University of California, Irvine, California, USA
S. Meinardi
Department of Chemistry, University of California, Irvine, California, USA
G. Sachse
NASA Langley Research Center, Hampton, Virginia, USA
C. Harward
NASA Langley Research Center, Hampton, Virginia, USA
T.-Y. Chen
Environmental Change Research Project, Academia Sinica, Taipei, Taiwan
D. Thornton
Department of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA
F.-H. Tu
Department of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA
A. Bandy
Department of Chemistry, Drexel University, Philadelphia, Pennsylvania, USA
Abstract
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
+, SO4
2−, 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 SO4
2− dominated, with the dust-derived Ca2+ contributing nearly equally as SO4
2− 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 SO4
2−, 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
+, SO4
2−, 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[SO4
2−]) ratio was ∼0.70 in the two campaigns, with deviations found only in volcano plumes, whereby SO4
2− 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.
Received 1
December
2002;
accepted 28
March
2003;
published 13
September
2003.
Index Terms: 0305 Atmospheric Composition and Structure: Aerosols and particles (0345, 4801); 0322 Atmospheric Composition and Structure: Constituent sources and sinks; 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry; 0368 Atmospheric Composition and Structure: Troposphere—constituent transport and chemistry; 0394 Atmospheric Composition and Structure: Instruments and techniques.
Read Full Article (file size: 3328334 bytes) Cited by
Citation: Lee, Y.-N., et al.
(2003),
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,
J. Geophys. Res.,
108(D23),
8646,
doi:10.1029/2002JD003265.
Copyright 2003 by the American Geophysical Union.
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