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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

Aging of Organic Aerosol: Bridging the Gap Between Laboratory and Field Studies

TL;DR: Data suggest that although matrix effects identified in the laboratory have taken a step toward reconciling laboratory-field disagreements, further work is needed to understand the actual aging rates of organics in ambient particles.
Journal ArticleDOI

Elemental Analysis of Organic Species with Electron Ionization High-Resolution Mass Spectrometry

TL;DR: A new elemental analysis (EA) technique for organic species (CHNO) that allows fast on-line analysis (10 s) and reduces the required sample size to approximately 1 ng, approximately 6 orders of magnitude less than standard techniques.
Journal ArticleDOI

Calibration and measurement uncertainties of a continuous-flow cloud condensation nuclei counter (DMT-CCNC): CCN activation of ammonium sulfate and sodium chloride aerosol particles in theory and experiment

TL;DR: In this paper, the experimental and theoretical uncertainties in the measurement of cloud condensation nuclei (CCN) with a continuous-flow thermal-gradient CCN counter from Droplet Measurement Technologies (DMT-CCNC) have been assessed by model calculations and calibration experiments with ammonium sulfate and sodium chloride aerosol particles in the diameter range of 20-220 nm.
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