4.7 Article

Hygroscopic properties and cloud condensation nuclei activation of limonene-derived organosulfates and their mixtures with ammonium sulfate

Journal

ATMOSPHERIC CHEMISTRY AND PHYSICS
Volume 15, Issue 24, Pages 14071-14089

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-15-14071-2015

Keywords

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Funding

  1. NordForsk (Nordic Council of Ministers) through the Nordic Centre of Excellence Cryosphere-Atmosphere Interactions in a Changing Arctic Climate (CRAICC)
  2. VILLUM Foundation
  3. European Union Seventh Framework Programme [262254]
  4. Office of Science (BER), US Department of Energy via Biogenic Aerosols - Effects on Clouds and Climate (BAECC)
  5. Finnish Academy of Sciences [257411]
  6. ERC [QAPPA 335478]
  7. Academy Grant [259005]

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Organosulfates have been observed as constituents of atmospheric aerosols in a wide range of environments; however their hygroscopic properties remain uncharacterised. Here, limonene-derived organosulfates with a molecular weight of 250 Da (L-OS 250) were synthesised and used for simultaneous measurements with a hygroscopicity tandem differential mobility analyser (H-TDMA) and a cloud condensation nuclei counter (CCNC) to determine the hygroscopicity parameter, kappa, for pure L-OS 250 and mixtures of L-OS 250 with ammonium sulfate (AS) over a wide range of humidity conditions. The kappa values derived from measurements with H-TDMA decreased with increasing particle dry diameter for all chemical compositions investigated, indicating that kappa H-TDMA depends on particle diameter and/or surface effects; however, it is not clear if this trend is statistically significant. For pure L-OS 250, kappa was found to increase with increasing relative humidity, indicating dilution/solubility effects to be significant. Discrepancies in kappa between the sub-and supersaturated measurements were observed for LOS 250, whereas kappa of AS and mixed L-OS 250/AS were similar. This discrepancy was primarily ascribed to limited dissolution of L-OS 250 at subsaturated conditions. In general, hygroscopic growth factor, critical particle diameter and kappa for the mixed L-OS 250/AS particles converged towards the values of pure AS for mixtures with >= 20% w/w AS. Surface tension measurements of bulk aqueous L-OS 250/AS solutions showed that L-OS 250 was indeed surface active, as expected from its molecular structure, decreasing the surface tension of solutions with 24% from the pure water value at a L-OS 250 concentration of 0.0025 mol L-1. Based on these surface tension measurements, we present the first concentration-dependent parametrisation of surface tension for aqueous L-OS 250, which was implemented to different process-level models of L-OS 250 hygroscopicity and CCN activation. The values of kappa obtained from the measurements were compared with kappa calculated applying the volume additive Zdanovskii-Stokes-Robinson mixing rule, as well as kappa modelled from equilibrium Kohler theory with different assumptions regarding L-OS 250 bulk-to-surface partitioning and aqueous droplet surface tension. This study is to our knowledge the first to investigate the hygroscopic properties and surface activity of L-OS 250; hence it is an important first step towards understanding the atmospheric impact of organosulfates.

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