Review of ‘Heterogeneous Ice Nucleation Properties of Natural Desert Dust Particles Coated with a Surrogate of Secondary Organic Aerosol’

2018 ◽  
Author(s):  
Anonymous
Keyword(s):  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Desert Dust ◽  
Heterogeneous Ice Nucleation

scholarly journals Heterogeneous ice nucleation of viscous secondary organic aerosol produced from ozonolysis of <i>α</i>-pinene

2016 ◽  
Vol 16 (10) ◽  
pp. 6495-6509 ◽  
Author(s):  
Karoliina Ignatius ◽  
Thomas B. Kristensen ◽  
Emma Järvinen ◽  
Leonid Nichman ◽  
Claudia Fuchs ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Solid Phase ◽  
Particle Surface ◽  
Amorphous Solid ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Cloud Formation ◽  
Particle Surface Area ◽  
Semi Solid ◽  
Heterogeneous Ice Nucleation

Abstract. There are strong indications that particles containing secondary organic aerosol (SOA) exhibit amorphous solid or semi-solid phase states in the atmosphere. This may facilitate heterogeneous ice nucleation and thus influence cloud properties. However, experimental ice nucleation studies of biogenic SOA are scarce. Here, we investigated the ice nucleation ability of viscous SOA particles. The SOA particles were produced from the ozone initiated oxidation of α-pinene in an aerosol chamber at temperatures in the range from −38 to −10 °C at 5–15 % relative humidity with respect to water to ensure their formation in a highly viscous phase state, i.e. semi-solid or glassy. The ice nucleation ability of SOA particles with different sizes was investigated with a new continuous flow diffusion chamber. For the first time, we observed heterogeneous ice nucleation of viscous α-pinene SOA for ice saturation ratios between 1.3 and 1.4 significantly below the homogeneous freezing limit. The maximum frozen fractions found at temperatures between −39.0 and −37.2 °C ranged from 6 to 20 % and did not depend on the particle surface area. Global modelling of monoterpene SOA particles suggests that viscous biogenic SOA particles are indeed present in regions where cirrus cloud formation takes place. Hence, they could make up an important contribution to the global ice nucleating particle budget.

scholarly journals Heterogeneous Ice Nucleation on Simulated Secondary Organic Aerosol

2014 ◽  
Vol 48 (3) ◽  
pp. 1675-1682 ◽  
Author(s):  
Gregory P. Schill ◽  
David O. De Haan ◽  
Margaret A. Tolbert
Keyword(s):  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Heterogeneous Ice Nucleation

scholarly journals Heterogeneous ice nucleation of viscous secondary organic aerosol produced from ozonolysis of α-pinene

2015 ◽  
Vol 15 (24) ◽  
pp. 35719-35752 ◽  
Author(s):  
K. Ignatius ◽  
T. B. Kristensen ◽  
E. Järvinen ◽  
L. Nichman ◽  
C. Fuchs ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Solid Phase ◽  
Particle Surface ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Cloud Formation ◽  
Cirrus Cloud ◽  
Particle Surface Area ◽  
Semi Solid ◽  
Heterogeneous Ice Nucleation

Abstract. There are strong indications that particles containing secondary organic aerosol (SOA) exhibit amorphous solid or semi-solid phase states in the atmosphere. This may facilitate deposition ice nucleation and thus influence cirrus cloud properties. However, experimental ice nucleation studies of biogenic SOA are scarce. Here, we investigated the ice nucleation ability of viscous SOA particles. The SOA particles were produced from the ozone initiated oxidation of α-pinene in an aerosol chamber at temperatures in the range from −38 to −10 °C at 5–15 % relative humidity with respect to water to ensure their formation in a highly viscous phase state, i.e. semi-solid or glassy. The ice nucleation ability of SOA particles with different sizes was investigated with a new continuous flow diffusion chamber. For the first time, we observed heterogeneous ice nucleation of viscous α-pinene SOA in the deposition mode for ice saturation ratios between 1.3 and 1.4 significantly below the homogeneous freezing limit. The maximum frozen fractions found at temperatures between −36.5 and −38.3 °C ranged from 6 to 20 % and did not depend on the particle surface area. Global modelling of monoterpene SOA particles suggests that viscous biogenic SOA particles are indeed present in regions where cirrus cloud formation takes place. Hence, they could make up an important contribution to the global ice nuclei (IN) budget.

scholarly journals The efficiency of secondary organic aerosol particles to act as ice nucleating particles at mixed-phase cloud conditions

2018 ◽  
Author(s):  
Wiebke Frey ◽  
Dawei Hu ◽  
James Dorsey ◽  
M. Rami Alfarra ◽  
Aki Pajunoja ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Aerosol Particles ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Dust Particles ◽  
Ice Cloud ◽  
Liquid Saturation ◽  
Reference Experiment ◽  
Mixed Phase Clouds

Abstract. Secondary Organic Aerosol (SOA) particles have been found to be efficient ice nucleating particles under the cold conditions of (tropical) upper tropospheric cirrus clouds. Whether they also are efficient at initiating freezing at slightly warmer conditions as found in mixed phase clouds remains undetermined. Here, we study the ice nucleating ability of photo-chemically produced SOA particles with the combination of the Manchester Aerosol and Ice Cloud Chambers. Three SOA systems were tested resembling biogenic/anthropogenic particles and particles of different phase state. After the aerosol particles were formed, they were transferred into the cloud chamber where subsequent quasi-adiabatic cloud evacuations were performed. Additionally, the ice forming abilities of ammonium sulfate and kaolinite were investigated as a reference to test the experimental setup. Clouds were formed in the temperature range of −20 °C to −28.6 °C. Only the reference experiment using dust particles showed evidence of ice nucleation. No ice particles were observed in any other experiment. Thus, we conclude that SOA particles produced under the conditions of the reported experiments are not efficient ice nucleating particles starting at liquid saturation under mixed-phase cloud conditions.

scholarly journals Heterogeneous ice nucleation properties of natural desert dust particles coated with a surrogate of secondary organic aerosol

2019 ◽  
Vol 19 (7) ◽  
pp. 5091-5110 ◽  
Author(s):  
Zamin A. Kanji ◽  
Ryan C. Sullivan ◽  
Monika Niemand ◽  
Paul J. DeMott ◽  
Anthony J. Prenni ◽  
...  
Keyword(s):  
Coating Thickness ◽  
Secondary Organic Aerosol ◽  
Mineral Dust ◽  
Size Fraction ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Expansion Chamber ◽  
Significant Difference ◽  
Immersion Freezing

Abstract. Ice nucleation abilities of surface collected mineral dust particles from the Sahara (SD) and Asia (AD) are investigated for the temperature (T) range 253–233 K and for supersaturated relative humidity (RH) conditions in the immersion freezing regime. The dust particles were also coated with a proxy of secondary organic aerosol (SOA) from the dark ozonolysis of α-pinene to better understand the influence of atmospheric coatings on the immersion freezing ability of mineral dust particles. The measurements are conducted on polydisperse particles in the size range 0.01–3 µm with three different ice nucleation chambers. Two of the chambers follow the continuous flow diffusion chamber (CFDC) principle (Portable Ice Nucleation Chamber, PINC) and the Colorado State University CFDC (CSU-CFDC), whereas the third was the Aerosol Interactions and Dynamics in the Atmosphere (AIDA) cloud expansion chamber. From observed activated fractions (AFs) and ice nucleation active site (INAS) densities, it is concluded within experimental uncertainties that there is no significant difference between the ice nucleation ability of the particular SD and AD samples examined. A small bias towards higher INAS densities for uncoated versus SOA-coated dusts is found but this is well within the 1σ (66 % prediction bands) region of the average fit to the data, which captures 75 % of the INAS densities observed in this study. Furthermore, no systematic differences are observed between SOA-coated and uncoated dusts in both SD and AD cases, regardless of coating thickness (3–60 nm). The results suggest that any differences observed are within the uncertainty of the measurements or differences in cloud chamber parameters such as size fraction of particles sampled, and residence time, as well as assumptions in using INAS densities to compare polydisperse aerosol measurements which may show variable composition with particle size. Coatings with similar properties to that of the SOA in this work and with coating thickness up to 60 nm are not expected to impede or enhance the immersion mode ice nucleation ability of mineral dust particles.

scholarly journals Heterogeneous Ice Nucleation Properties of Natural Desert Dust Particles Coated with a Surrogate of Secondary Organic Aerosol

2018 ◽  
Author(s):  
Zamin A. Kanji ◽  
Ryan C. Sullivan ◽  
Monika Niemand ◽  
Paul J. DeMott ◽  
Anthony J. Prenni ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Mineral Dust ◽  
Size Fraction ◽  
Diffusion Chamber ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Expansion Chamber ◽  
Significant Difference ◽  
Immersion Freezing

Abstract. Ice nucleation abilities of surface collected mineral dust particles from the Sahara (SD) and Asia (AD) are investigated for the temperature range 253–233 K and for supersaturated humidity conditions in the immersion-freezing regime. The dust particles were also coated with a proxy of secondary organic aerosol (SOA) from the dark ozonolysis of α-pinene to better understand the influence of atmospheric coatings on the immersion freezing ability of mineral dust particles. The measurements are conducted on poly-disperse particles in the size range 0.01–3 µm with three different ice nucleation chambers. Two of the chambers follow the continuous flow diffusion chamber (CFDC) principle (Portable Ice Nucleation Chamber, PINC) and the Colorado State University CFDC (CSU-CFDC), whereas the third was the Aerosol Interactions and Dynamics in the Atmosphere (AIDA) cloud expansion chamber. From observed activated fractions (AF) and ice nucleation active site (INAS) densities, it is concluded within experimental uncertainties that there is no significant difference between the ice nucleation ability of the particular SD and AD samples examined. A small bias towards higher INAS densities for uncoated versus SOA coated dusts is found but this is well within the 1σ (66 % prediction bands) region of the average fit to the data, which captures 75 % of the INAS densities observed in this study. Furthermore, no systematic differences are observed between SOA coated and uncoated dusts in both SD and AD cases, regardless of coating thickness (3–60 nm). The results suggest that differences observed are mostly within the uncertainty of the measurements or differences in cloud chamber parameters such as size fraction of particles sampled, and residence time, as well as assumptions in using INAS densities to compare poly-disperse aerosol measurements which may show variable composition with particle size. In the atmosphere, coatings with similar properties to that of the SOA tested here for a thickness up to 60 nm, the maximum thickness tested here, is not expected to impede or enhance the ice nucleation ability by immersion mode of mineral dust in the mixed-phase cloud regime.

scholarly journals Heterogeneous ice nucleation measurements of secondary organic aerosol generated from ozonolysis of alkenes

2009 ◽  
Vol 36 (6) ◽  
Author(s):  
Anthony J. Prenni ◽  
Markus D. Petters ◽  
Annelise Faulhaber ◽  
Christian M. Carrico ◽  
Paul J. Ziemann ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Heterogeneous Ice Nucleation

scholarly journals Small ice particles at slightly supercooled temperatures in tropical maritime convection

2020 ◽  
Vol 20 (6) ◽  
pp. 3895-3904
Author(s):  
Gary Lloyd ◽  
Thomas Choularton ◽  
Keith Bower ◽  
Jonathan Crosier ◽  
Martin Gallagher ◽  
...  
Keyword(s):  
Ice Nucleation ◽  
Dust Particles ◽  
Cumulus Clouds ◽  
Desert Dust ◽  
Ice Nuclei ◽  
Production Processes ◽  
Ice Particles ◽  
Small Crystals ◽  
Vapour Diffusion ◽  
Very High

Abstract. In this paper we show that the origin of the ice phase in tropical cumulus clouds over the sea may occur by primary ice nucleation of small crystals at temperatures just between 0 and −5 ∘C. This was made possible through use of a holographic instrument able to image cloud particles at very high resolution and small size (6 µm). The environment in which the observations were conducted was notable for the presence of desert dust advected over the ocean from the Sahara. However, there is no laboratory evidence to suggest that these dust particles can act as ice nuclei at temperatures warmer than about −10 ∘C, the zone in which the first ice was observed in these clouds. The small ice particles were observed to grow rapidly by vapour diffusion, riming, and possibly through collisions with supercooled raindrops, causing these to freeze and potentially shatter. This in turn leads to the further production of secondary ice in these clouds. Hence, although the numbers of primary ice particles are small, they are very effective in initiating the rapid glaciation of the cloud, altering the dynamics and precipitation production processes.

scholarly journals Heterogeneous ice nucleation on dust particles sourced from nine deserts worldwide – Part 2: Deposition nucleation and condensation freezing

2019 ◽  
Vol 19 (2) ◽  
pp. 1059-1076 ◽  
Author(s):  
Yvonne Boose ◽  
Philipp Baloh ◽  
Michael Plötze ◽  
Johannes Ofner ◽  
Hinrich Grothe ◽  
...  
Keyword(s):  
Active Sites ◽  
Mineral Dust ◽  
Atmospheric Transport ◽  
Chemical Imaging ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Full Potential ◽  
Nucleation Behavior ◽  
Crystal Water ◽  
Desert Dust

Abstract. Mineral dust particles from deserts are amongst the most common ice nucleating particles in the atmosphere. The mineralogy of desert dust differs depending on the source region and can further fractionate during the dust emission processes. Mineralogy to a large extent explains the ice nucleation behavior of desert aerosol, but not entirely. Apart from pure mineral dust, desert aerosol particles often exhibit a coating or are mixed with small amounts of biological material. Aging on the ground or during atmospheric transport can deactivate nucleation sites, thus strong ice nucleating minerals may not exhibit their full potential. In the partner paper of this work, it was shown that mineralogy determines most but not all of the ice nucleation behavior in the immersion mode found for desert dust. In this study, the influence of semi-volatile organic compounds and the presence of crystal water on the ice nucleation behavior of desert aerosol is investigated. This work focuses on the deposition and condensation ice nucleation modes at temperatures between 238 and 242 K of 18 dust samples sourced from nine deserts worldwide. Chemical imaging of the particles' surface is used to determine the cause of the observed differences in ice nucleation. It is found that, while the ice nucleation ability of the majority of the dust samples is dominated by their quartz and feldspar content, in one carbonaceous sample it is mostly caused by organic matter, potentially cellulose and/or proteins. In contrast, the ice nucleation ability of an airborne Saharan sample is found to be diminished, likely by semi-volatile species covering ice nucleation active sites of the minerals. This study shows that in addition to mineralogy, other factors such as organics and crystal water content can alter the ice nucleation behavior of desert aerosol during atmospheric transport in various ways.

Sign in / Sign up

Export Citation Format

Share Document