Author(s)
| Bertozzi, Barbara (KIT, Karlsruhe) ; Wagner, Robert (KIT, Karlsruhe) ; Song, Junwei (KIT, Karlsruhe) ; Höhler, Kristina (KIT, Karlsruhe) ; Pfeifer, Joschka (CERN) ; Saathoff, Harald (KIT, Karlsruhe) ; Leisner, Thomas (KIT, Karlsruhe) ; Möhler, Ottmar (KIT, Karlsruhe) |
Abstract
| The abundance of aerosol particles and their ability to catalyze ice nucleation are key parameters to correctly
understand and describe the aerosol indirect effect on the climate. Cirrus clouds strongly influence the Earth’s radiative
budget, but their effect is highly sensitive to their formation
mechanism, which is still poorly understood. Sulfate and organics are among the most abundant aerosol components in
the troposphere and have also been found in cirrus ice crystal residuals. Most of the studies on ice nucleation at cirrus
cloud conditions looked at either purely inorganic or purely
organic particles. However, particles in the atmosphere are
mostly found as internal mixtures, the ice nucleation ability
of which is not yet fully characterized.
In this study, we investigated the ice nucleation ability of
internally mixed particles composed of crystalline ammonium sulfate (AS) and secondary organic material (SOM)
at temperatures between −50 and −65 ◦C. The SOM was
generated from the ozonolysis of α-pinene. The experiments
were conducted in a large cloud chamber, which also allowed us to simulate various aging processes that the particles may experience during their transport in the atmosphere, like cloud cycling and redistribution of the organic
matter. We found that the ice nucleation ability of the mixed
AS / SOM particles is strongly dependent on the particle morphology. Small organic mass fractions of 5 wt %–8 wt % condensed on the surface of AS crystals are sufficient to completely suppress the ice nucleation ability of the inorganic
component, suggesting that the organic coating is evenly distributed on the surface of the seed particles. In this case, the
ice nucleation onset increased from a saturation ratio with respect to ice Sice ∼ 1.30 for the pure AS crystals to ≥ 1.45 for
the SOM-coated AS crystals. However, if such SOM-coated
AS crystals are subjected to the mentioned aging processes,
they show an improved ice nucleation ability with the ice
nucleation onset at Sice ∼ 1.35. We suggest that the aging
processes change the particle morphology. The organic matter might redistribute on the surface to form a partially engulfed structure, where the ice-nucleation-active sites of the
AS crystals are no longer completely masked by the organic
coating, or the morphology of the organic coating layer might
transform from a compact to a porous structure.
Our results underline the complexity in representing the
ice nucleation ability of internally mixed particles in cloud
models. They also demonstrate the need to further investigate
the impact of atmospheric aging and cloud processing on the
morphology and related ice nucleation ability of internally
mixed particles. |