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      On the formation of sulphuric acid – amine clusters in varying atmospheric conditions and its influence on atmospheric new particle formation

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          Abstract

          <p><strong>Abstract.</strong> Sulphuric acid is a key component in atmospheric new particle formation. However, sulphuric acid alone does not form stable enough clusters to initiate particle formation in atmospheric conditions. Strong bases, such as amines, have been suggested to stabilize sulphuric acid clusters and thus participate in particle formation. We modelled the formation rate of clusters with two sulphuric acid and two amine molecules (<i>J</i><sub>A2B2</sub>) at varying atmospherically relevant conditions with respect to concentrations of sulphuric acid ([H<sub>2</sub>SO<sub>4</sub>]), dimethylamine ([DMA]) and trimethylamine ([TMA]), temperature and relative humidity (RH). We also tested how the model results change if we assume that the clusters with two sulphuric acid and two amine molecules would act as seeds for heterogeneous nucleation of organic vapours (other than amines) with higher atmospheric concentrations than sulphuric acid. The modelled formation rates <i>J</i><sub>A2B2</sub> were functions of sulphuric acid concentration with close to quadratic dependence, which is in good agreement with atmospheric observations of the connection between the particle formation rate and sulphuric acid concentration. The coefficients <i>K</i><sub>A2B2</sub> connecting the cluster formation rate and sulphuric acid concentrations as <i>J</i><sub>A2B2</sub>=<i>K</i><sub>A2B2</sub>[H<sub>2</sub>SO<sub>4</sub>]<sup>2</sup> turned out to depend also on amine concentrations, temperature and relative humidity. We compared the modelled coefficients <i>K</i><sub>A2B2</sub> with the corresponding coefficients calculated from the atmospheric observations (<i>K</i><sub>obs</sub>) from environments with varying temperatures and levels of anthropogenic influence. By taking into account the modelled behaviour of <i>J</i><sub>A2B2</sub> as a function of [H<sub>2</sub>SO<sub>4</sub>], temperature and RH, the atmospheric particle formation rate was reproduced more closely than with the traditional semi-empirical formulae based on sulphuric acid concentration only. The formation rates of clusters with two sulphuric acid and two amine molecules with different amine compositions (DMA or TMA or one of both) had different responses to varying meteorological conditions and concentrations of vapours participating in particle formation. The observed inverse proportionality of the coefficient <i>K</i><sub>obs</sub> with RH and temperature agreed best with the modelled coefficient <i>K</i><sub>A2B2</sub> related to formation of a cluster with two H<sub>2</sub>SO<sub>4</sub> and one or two TMA molecules, assuming that these clusters can grow in collisions with abundant organic vapour molecules. In case this assumption is valid, our results suggest that the formation rate of clusters with at least two of both sulphuric acid and amine molecules might be the rate-limiting step for atmospheric particle formation. More generally, our analysis elucidates the sensitivity of the atmospheric particle formation rate to meteorological variables and concentrations of vapours participating in particle formation (also other than H<sub>2</sub>SO<sub>4</sub>).</p>

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          Nucleation and growth of nanoparticles in the atmosphere.

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              The Role of Sulfuric Acid in Atmospheric Nucleation

              Nucleation is a fundamental step in atmospheric new-particle formation. However, laboratory experiments on nucleation have systematically failed to demonstrate sulfuric acid particle formation rates as high as those necessary to account for ambient atmospheric concentrations, and the role of sulfuric acid in atmospheric nucleation has remained a mystery. Here, we report measurements of new particles (with diameters of approximately 1.5 nanometers) observed immediately after their formation at atmospherically relevant sulfuric acid concentrations. Furthermore, we show that correlations between measured nucleation rates and sulfuric acid concentrations suggest that freshly formed particles contain one to two sulfuric acid molecules, a number consistent with assumptions that are based on atmospheric observations. Incorporation of these findings into global models should improve the understanding of the impact of secondary particle formation on climate.
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                Author and article information

                Journal
                Atmospheric Chemistry and Physics
                Atmos. Chem. Phys.
                Copernicus GmbH
                1680-7324
                2012
                October 05 2012
                : 12
                : 19
                : 9113-9133
                Article
                10.5194/acp-12-9113-2012
                d4b3b63a-e0e0-4781-abee-113801054041
                © 2012

                https://creativecommons.org/licenses/by/3.0/

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