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CCN closure study: Effects of aerosol chemical composition and mixing state

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TLDR
In this article, the effects of chemical composition (bulk and size resolved) and mixing state (internal and external) on CCN activity of aerosols were investigated during the winter season in Kanpur.
Abstract
This study presents a detailed cloud condensation nuclei (CCN) closure study that investigates the effects of chemical composition (bulk and size resolved) and mixing state (internal and external) on CCN activity of aerosols. Measurements of the chemical composition, aerosol size distribution, total number concentration, and CCN concentration at supersaturation (SS = 0.2–1.0%) were performed during the winter season in Kanpur, India. Among the two cases considered here, better closure results are obtained for case 1 (low total aerosol loading, 49.54 ± 26.42 μg m−3, and high O:C ratio, 0.61 ± 0.07) compared to case 2 (high total aerosol loading, 101.05 ± 18.73 μg m−3, and low O:C ratio, 0.42 ± 0.06), with a maximum reduction of 3–81% in CCN overprediction for all depleted SS values (0.18–0.60%). Including the assumption that less volatile oxidized organic aerosols represent the soluble organic fraction reduced the overprediction to at most 40% and 129% in the internal and external mixing scenarios, respectively. At higher depleted SS values (0.34–0.60%), size-resolved chemical composition with an internal mixing state performed well in CCN closure among all organic solubility scenarios. However, at a lower depleted SS value (0.18%), closure is found to be more sensitive to both the chemical composition and mixing state of aerosols. At higher SS values, information on the solubility of organics and size-resolved chemical composition is required for accurate CCN predictions, whereas at lower SS values, information on the mixing state in addition to the solubility of organics and size-resolved chemical composition is required. Overall, κtotal values are observed to be independent of the O:C ratio [κtotal = (0.36 ± 0.01) × O:C − (0.03 ± 0.01)] in the range of 0.2<O:C<0.81, which indicates that the variation in the chemical composition of aerosols is not well represented by the changes in the O:C ratio alone.

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Citations
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Particle hygroscopicity and its link to chemical composition in the urban atmosphere of Beijing, China, during summertime

TL;DR: In this article, the mean hygroscopicity parameters (κs) of 50, 100, 150, 200, and 250 nm particles were respectively 0.16, 0.19, p.07 and 0.10, showing an increasing trend with increasing particle size.
Journal ArticleDOI

A review of aerosol chemistry in Asia: insights from aerosol mass spectrometer measurements

TL;DR: Aerosol composition varied largely in different regions, but was overall dominated by organic aerosols (OA, 32-75%), especially in south and southeast Asia due to the impact of biomass burning, and secondary OA was a ubiquitous and dominant aerosol component in all regions.
Journal ArticleDOI

Real-time measurements of ambient aerosols in a polluted Indian city: Sources, characteristics, and processing of organic aerosols during foggy and nonfoggy periods

TL;DR: In this article, a detailed time-resolved chemical characterization of ambient nonrefractory submicron aerosols (NR-PM1) was conducted for the first time in India.
References
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Journal ArticleDOI

A Case Study of Urban Particle Acidity and Its Influence on Secondary Organic Aerosol

TL;DR: Size-resolved indicators of aerosol acidity, including H+ ion concentrations (H+Aer) and the ratio of stoichiometric neutralization and the mass concentrations and size distributions of oxygenated organic aerosol (00A--surrogate for SOA in Pittsburgh) are evaluated, suggesting that the chemical nature of SOA is similar during acidic and neutralized periods and that there is no significant enhancement of SoA oligomer formation during acidic particle periods in Pittsburgh.
Journal ArticleDOI

Laboratory studies of the chemical composition and cloud condensation nuclei (CCN) activity of secondary organic aerosol (SOA) and oxidized primary organic aerosol (OPOA)

TL;DR: In this paper, secondary organic aerosol (SOA) and oxidized OPOA were generated via controlled exposure of precursors to OH radicals and/or O 3 in a potential aerosol mass (PAM) flow reactor over timescales equivalent to 1-20 days of atmospheric aging.
Journal ArticleDOI

Oxygenated and water-soluble organic aerosols in Tokyo

TL;DR: In this paper, an Aerodyne aerosol mass spectrometer (AMS) and a particle-into-liquid sampler (PILS) were used to measure water-soluble organic carbon (WSOC) during the winter and summer of 2004 in Tokyo.
Journal ArticleDOI

Measurement of ambient aerosols in northern Mexico City by single particle mass spectrometry

TL;DR: In this paper, a clock of hourly changes in single parti- cle mixing state and sources as a function of meteorology in Mexico City is presented. But the results are limited to 15-27 March 2006, when the data were collected in an industrial/residential section in the northern part of Mexico City.
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