Abstract

Abstract. The link between measured sub-saturated hygroscopicity and cloud activation potential of secondary organic aerosol particles produced by the chamber photo-oxidation of α-pinene in the presence or absence of ammonium sulphate seed aerosol was investigated using two models of varying complexity. A simple single hygroscopicity parameter model and a more complex model (incorporating surface effects) were used to assess the detail required to predict the cloud condensation nucleus (CCN) activity from the sub-saturated water uptake. Sub-saturated water uptake measured by three hygroscopicity tandem differential mobility analyser (HTDMA) instruments was used to determine the water activity for use in the models. The predicted CCN activity was compared to the measured CCN activation potential using a continuous flow CCN counter. Reconciliation using the more complex model formulation with measured cloud activation could be achieved widely different assumed surface tension behavior of the growing droplet; this was entirely determined by the instrument used as the source of water activity data. This unreliable derivation of the water activity as a function of solute concentration from sub-saturated hygroscopicity data indicates a limitation in the use of such data in predicting cloud condensation nucleus behavior of particles with a significant organic fraction. Similarly, the ability of the simpler single parameter model to predict cloud activation behaviour was dependent on the instrument used to measure sub-saturated hygroscopicity and the relative humidity used to provide the model input. However, agreement was observed for inorganic salt solution particles, which were measured by all instruments in agreement with theory. The difference in HTDMA data from validated and extensively used instruments means that it cannot be stated with certainty the detail required to predict the CCN activity from sub-saturated hygroscopicity. In order to narrow the gap between measurements of hygroscopic growth and CCN activity the processes involved must be understood and the instrumentation extensively quality assured. It is impossible to say from the results presented here due to the differences in HTDMA data whether: i) Surface tension suppression occurs ii) Bulk to surface partitioning is important iii) The water activity coefficient changes significantly as a function of the solute concentration.

Highlights

  • Aerosol in the atmosphere comprises numerous and diverse components originating from both natural and anthropogenic activities

  • It is impossible to say from the results presented here due to the differences in hygroscopicity tandem differential mobility analyser (HTDMA) data whether: i) Surface tension suppression occurs ii) Bulk to surface partitioning is important iii) The water activity coefficient changes significantly as a function of the solute concentration

  • Predictions made from HPSI compare well using either the Aerosol Diameter Dependent Equilibrium Model (ADDEM) model and assuming the surface tension of water or the κ-model

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Summary

Introduction

Aerosol in the atmosphere comprises numerous and diverse components originating from both natural and anthropogenic activities. The composition of secondary organic aerosol (SOA) in the atmosphere is complex and this may be expected to propagate into the properties and behavior. Since it may comprise a large fraction of the ambient aerosol, SOA will significantly contribute to the aerosol direct and indirect effects on climate and weather (Haywood and Boucher, 2000; Forster et al, 2007). It is necessary to quantify the optical properties, hygroscopicity and cloud droplet activation behavior of SOA and how they relate to each other. The relationship between these last two properties is the focus of this work

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