Rapid measurement of particle hygroscopicity and CCN activity using broad scanning supersaturation (BS2)-CCNC: calibration and intercomparison

Author(s):  
Najin Kim ◽  
Yafang Cheng ◽  
Nan Ma ◽  
Mira Pöhlker ◽  
Thomas Klimach ◽  
...  

<p>For understanding and assessing aerosol-cloud interactions and their impact on climate, reliable measurement data of aerosol particle hygroscopicity and cloud condensation nuclei (CCN) activity are required. Furthermore, aerosol liquid water, mainly controlled by hygroscopicity, affects heterogeneous and multiphase reactions of aerosol particles. The CCN activity of aerosol particles can be determined by scanning particle size and supersaturation (S) in the CCN measurement. Compared to the existing CCN activity measurement, a broad supersaturation scanning CCN (BS2-CCN) system, in which particles are exposed to a range of S simultaneously, can measure particle hygroscopicity and CCN activity with a high-time resolution. Based on a monotonic relation between the activation supersaturation of aerosol particles (S<sub>aerosol</sub>)  and the activation fraction (F<sub>act</sub>) of the BS2-CCN measurement, we can derive κ, a single hygroscopicity parameter, directly.</p><p>Here, we describe how the BS2-CCN system can be effectively calibrated and which factors can affect the calibration curve (F<sub>act</sub> - S<sub>aerosol</sub>). For calibration, size-resolved CCN measurements with ammonium sulfate (AS) and sodium chloride particles are performed under the three different thermal gradient (dT) conditions (dT=6, 8, and 10). First, the shape of the calibration curve is primarily influenced by S<sub>max</sub>, maximum S in the activation tube. We need to determine appropriate S<sub>max</sub> depending on particle size and κ to be investigated. To minimize the effect of double/multiple charged particles, small  D<sub>g </sub>and σ<sub>g</sub>  in number size distribution are recommended when generating the calibration aerosols. Sheath-to-aerosol-flow ratio (SAR) is the third factor to be considered. BS2-CCNC system uses a low SAR with a wider inlet compared to the typical CCN measurement, which can make a monotonic relation between F<sub>act</sub> and S<sub>aerosol</sub>. Lastly, F<sub>act </sub>is affected by particle number concentration and has a decreasing rate of 0.02/100 cm<sup>-3</sup> (within N<sub>CN</sub> ~ 300 cm<sup>-3</sup> for AS) due to the water consumption in the chamber. For evaluating the BS2-CCN system, inter-comparison experiments between typical DMA-CCN and BS2-CCN measurement were performed with the laboratory-generated aerosol mixture and ambient aerosols. Statistically good agreements of κ values between DMA-CCN and BS2-CCN measurements for both inter-comparison experiments imply that the BS2-CCN system can measure particle hygroscopicity and CCN activity well compared to the existing measurement. We expect that this new system can be applied to aircraft and ship measurements that require a high-time resolution as well as ground measurement for a broad range of hygroscopicity distribution. Because hygroscopicity is closely related to the fraction of organics/inorganics in aerosol particles, our method can also serve as a complementary approach for fast detection/estimation of aerosol chemical compositions. </p>

2021 ◽  
Author(s):  
Najin Kim ◽  
Yafang Cheng ◽  
Nan Ma ◽  
Mira L. Pöhlker ◽  
Thomas Klimach ◽  
...  

Abstract. For understanding and assessing aerosol-cloud interactions and their impact on climate, reliable measurement data of aerosol particle hygroscopicity and cloud condensation nuclei (CCN) activity are required. The CCN activity of aerosol particles can be determined by scanning particle size and supersaturation (S) in CCN measurements. Compared to the existing differential mobility analyzer (DMA)-CCN activity measurement, a broad supersaturation scanning CCN (BS2-CCN) system, in which particles are exposed to a range of S simultaneously, can measure the CCN activity with a high time-resolution. Based on a monotonic relation between the activation supersaturation of aerosol particles (Saerosol) and the activated fraction (Fact) of the BS2-CCN measurement, we can derive κ, a single hygroscopicity parameter, directly. Here, we describe how the BS2-CCN system can be effectively calibrated and which factors can affect the calibration curve (Fact – Saerosol). For calibration, size-resolved CCN measurements with ammonium sulfate and sodium chloride particles are performed under the three different thermal gradient (dT) conditions (dT = 6, 8, and 10 K). We point out key processes that can affect the calibration curve and thereby need to be considered as follows: First, the shape of the calibration curve is primarily influenced by Smax, the maximum S in the activation tube. We need to determine appropriate Smax depending on particle size and κ to be investigated. To minimize the effect of multiply charged particles, small geometric mean diameter (𝐷𝑔) and 𝜎𝑔 geometric standard deviation (𝜎𝑔) in number size distribution are recommended when generating the calibration aerosols. Last, Fact is affected by particle number concentration and has a decreasing rate of 0.02/100 cm−3 due to the water consumption in the activation tube. For evaluating the BS2-CCN system, inter-comparison experiments between typical DMA-CCN and BS2-CCN measurement were performed with the laboratory-generated aerosol mixture and ambient aerosols. Good agreements of κ values between DMA-CCN and BS2-CCN measurements for both experiments show that the BS2-CCN system can measure CCN activity well compared to the existing measurement, and can measure a broad range of hygroscopicity distribution with a high time-resolution (~1 second vs. few minutes for a standard CCN activity measurement). As the hygroscopicity can be used as a proxy for the chemical composition, our method can also serve as a complementary approach for fast and size-resolved detection/estimation of aerosol chemical composition.


2016 ◽  
Author(s):  
Dominik Stolzenburg ◽  
Gerhard Steiner ◽  
Paul M. Winkler

Abstract. Measurements of aerosol dynamics in the sub-10 nm size range are crucially important for quantifying the impact of new particle formation onto the global budget of cloud condensation nuclei. Here we present the development and characterization of a differential mobility analyzer – train (DMA-train), operating six DMAs in parallel for high time-resolution particle size-distribution measurements below 10 nm. The DMAs are operated at six different but fixed voltages and hence sizes, together with six state-of-the-art condensation particle counters. Two Airmodus A 10 particle size magnifiers (PSM) are used for channels below 2.5 nm while sizes above 2.5 nm are detected by TSI 3776 butanol or TSI 3788 water based CPCs. We report the transfer functions and characteristics of six identical Grimm S-DMAs as well as the calibration of a butanol-based TSI model 3776 CPC, a water-based TSI model 3788 CPC and an Aimodus A10 PSM. We find cut-off diameters similar to those reported in the literature. The performance of the DMA-train is tested with a rapidly changing aerosol of a tungsten oxide particle generator during warm-up. Additionally we report a measurement of new particle formation taken during a nucleation event in the CLOUD chamber experiment at CERN. We find that the DMA-train is able to bridge the gap between currently well-established measurement techniques in the cluster-particle transition regime, providing high time-resolution and accurate size information of neutral and charged particles even at atmospheric particle concentrations.


2017 ◽  
Vol 10 (4) ◽  
pp. 1639-1651 ◽  
Author(s):  
Dominik Stolzenburg ◽  
Gerhard Steiner ◽  
Paul M. Winkler

Abstract. Measurements of aerosol dynamics in the sub-10 nm size range are crucially important for quantifying the impact of new particle formation onto the global budget of cloud condensation nuclei. Here we present the development and characterization of a differential mobility analyzer train (DMA-train), operating six DMAs in parallel for high-time-resolution particle-size-distribution measurements below 10 nm. The DMAs are operated at six different but fixed voltages and hence sizes, together with six state-of-the-art condensation particle counters (CPCs). Two Airmodus A10 particle size magnifiers (PSM) are used for channels below 2.5 nm while sizes above 2.5 nm are detected by TSI 3776 butanol-based or TSI 3788 water-based CPCs. We report the transfer functions and characteristics of six identical Grimm S-DMAs as well as the calibration of a butanol-based TSI model 3776 CPC, a water-based TSI model 3788 CPC and an Airmodus A10 PSM. We find cutoff diameters similar to those reported in the literature. The performance of the DMA-train is tested with a rapidly changing aerosol of a tungsten oxide particle generator during warmup. Additionally we report a measurement of new particle formation taken during a nucleation event in the CLOUD chamber experiment at CERN. We find that the DMA-train is able to bridge the gap between currently well-established measurement techniques in the cluster–particle transition regime, providing high time resolution and accurate size information of neutral and charged particles even at atmospheric particle concentrations.


1994 ◽  
Vol 144 ◽  
pp. 431-434
Author(s):  
M. Minarovjech ◽  
M. Rybanský

AbstractThis paper deals with a possibility to use the ground-based method of observation in order to solve basic problems connected with the solar corona research. Namely:1.heating of the solar corona2.course of the global cycle in the corona3.rotation of the solar corona and development of active regions.There is stressed a possibility of high-time resolution of the coronal line photometer at Lomnický Peak coronal station, and use of the latter to obtain crucial observations.


2010 ◽  
Vol 180 (4) ◽  
pp. 424 ◽  
Author(s):  
G.M. Beskin ◽  
S.V. Karpov ◽  
S.F. Bondar ◽  
V.L. Plokhotnichenko ◽  
A. Guarnieri ◽  
...  

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