Abstract

Abstract. Sulfuric acid, amines and oxidized organics have been found to be important compounds in the nucleation and initial growth of atmospheric particles. Because of the challenges involved in determining the chemical composition of objects with very small mass, however, the properties of the freshly nucleated particles and the detailed pathways of their formation processes are still not clear. In this study, we focus on a challenging size range, i.e., particles that have grown to diameters of 10 and 15 nm following nucleation, and measure their water uptake. Water uptake is useful information for indirectly obtaining chemical composition of aerosol particles. We use a nanometer-hygroscopicity tandem differential mobility analyzer (nano-HTDMA) at subsaturated conditions (ca. 90 % relative humidity at 293 K) to measure the hygroscopicity of particles during the seventh Cosmics Leaving OUtdoor Droplets (CLOUD7) campaign performed at CERN in 2012. In CLOUD7, the hygroscopicity of nucleated nanoparticles was measured in the presence of sulfuric acid, sulfuric acid–dimethylamine, and sulfuric acid–organics derived from α-pinene oxidation. The hygroscopicity parameter κ decreased with increasing particle size, indicating decreasing acidity of particles. No clear effect of the sulfuric acid concentration on the hygroscopicity of 10 nm particles produced from sulfuric acid and dimethylamine was observed, whereas the hygroscopicity of 15 nm particles sharply decreased with decreasing sulfuric acid concentrations. In particular, when the concentration of sulfuric acid was 5.1 × 106 molecules cm−3 in the gas phase, and the dimethylamine mixing ratio was 11.8 ppt, the measured κ of 15 nm particles was 0.31 ± 0.01: close to the value reported for dimethylaminium sulfate (DMAS) (κDMAS ∼ 0.28). Furthermore, the difference in κ between sulfuric acid and sulfuric acid–imethylamine experiments increased with increasing particle size. The κ values of particles in the presence of sulfuric acid and organics were much smaller than those of particles in the presence of sulfuric acid and dimethylamine. This suggests that the organics produced from α-pinene ozonolysis play a significant role in particle growth even at 10 nm sizes.

Highlights

  • Aerosol particles can be directly emitted into the atmosphere from natural and anthropogenic sources or can be produced by gas-to-particle conversion processes

  • We focus on determining the hygroscopicity of nanoparticles generated by homogeneous nucleation of sulfuric acid with organic compounds such as dimethylamine and α-pinene oxidation products in the Cosmics Leaving OUtdoor Droplets (CLOUD) chamber at CERN

  • The hygroscopic properties of nucleated nanoparticles in the presence of sulfuric acid, sulfuric acid–dimethylamine, and sulfuric acid combined with organics derived from α-pinene ozonolysis were investigated with the nano-HTDMA

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Summary

Introduction

Aerosol particles can be directly emitted into the atmosphere from natural and anthropogenic sources (primary aerosols) or can be produced by gas-to-particle conversion processes (secondary aerosols) They affect the regional and global climate by absorbing and scattering light and by acting as cloud condensation nuclei (CCN) and ice nuclei (IN). It has been shown that new particle formation in the boundary layer cannot be explained by pure sulfuric acid–water nucleation (Kirkby et al, 2011). Other compounds such as ammonia and/or organics are needed to explain observed atmospheric particle formation and growth, and have been widely studied. Physicochemical properties of nanoparticles produced by homogeneous nucleation of amines with sulfuric acid–water and their subsequent growth are not yet well understood

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