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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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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.
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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.
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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

Aerosol hygroscopicity derived from size-segregated chemical composition and its parameterization in the North China Plain

TL;DR: In this article, the size-segregated aerosol particulate mass concentration as well as the particle components such as inorganic ions, organic carbon and water-soluble organic carbon (WSOC) are identified from aerosol particle samples collected with a ten-stage impactor.
Journal ArticleDOI

Cloud condensation nuclei closure during the International Consortium for Atmospheric Research on Transport and Transformation 2004 campaign: Effects of size-resolved composition

TL;DR: Medina et al. as discussed by the authors focused on the analysis of a week of measurements, during which semiurban and continental air were sampled, and the predictions of cloud condensation nuclei (CCN) concentrations were carried out using ''simple'' Kohler theory; the predictions are subsequently compared with CCN measurements at 0.8 ± 28.5% and 0.6% supersaturation.
Journal ArticleDOI

Chemical characterization of the ambient organic aerosol soluble in water: 1. Isolation of hydrophobic and hydrophilic fractions with a XAD-8 resin

TL;DR: In this article, the fraction of WSOC not retained by a XAD-8 resin column at pH 2 is termed as hydrophilic WSOC (WSOCxp); this includes aromatic acids, phenols, organic nitrates, cyclic acids, and carbonyls and monocarboxylic/dicarboxyslic acids with greater than 3 or 4 carbons.
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Carbonaceous and inorganic composition in long-range transported aerosols over northern Japan: Implication for aging of water-soluble organic fraction

TL;DR: In this paper, the authors collected atmospheric particles in Sapporo, northern Japan during spring and early summer 2005 under the air mass transport conditions from Siberia, China and surrounding seas, and analyzed for inorganic ions, organic carbon (OC), elemental carbon (EC), water-soluble organic carbon(WSOC), and the major water soluble organic compound classes (i.e., dicarboxylic acids and sugars).
Journal ArticleDOI

Analysis of CCN activity of Arctic aerosol and Canadian biomass burning during summer 2008

TL;DR: In this paper, a NASA DC-8 aircraft characterized the aerosol properties, chemical composition, and cloud condensation nuclei (CCN) concentrations of the summertime Arctic during the 2008 NASA Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) campaign.
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