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 <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 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 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 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 Viscous organic aerosol particles in the upper troposphere: diffusivity-controlled water uptake and ice nucleation?

2015 ◽  
Vol 15 (17) ◽  
pp. 24473-24511 ◽  
Author(s):  
D. M. Lienhard ◽  
A. J. Huisman ◽  
U. K. Krieger ◽  
Y. Rudich ◽  
C. Marcolli ◽  
...  
Keyword(s):  
Water Uptake ◽  
Condensed Phase ◽  
Aerosol Particles ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Water Diffusion ◽  
Tropical Tropopause ◽  
Phase Water ◽  
Very High ◽  
Heterogeneous Ice Nucleation

Abstract. New measurements of water diffusion in aerosol particles produced from secondary organic aerosol (SOA) material and from a number of organic/inorganic model mixtures (3-methylbutane-1,2,3-tricarboxylic acid (3-MBTCA), levoglucosan, levoglucosan/NH4HSO4, raffinose) indicate that water diffusion coefficients are determined by several properties of the aerosol substance and cannot be inferred from the glass transition temperature or bouncing properties. Our results suggest that water diffusion in SOA particles is faster than often assumed and imposes no significant kinetic limitation on water uptake and release at temperatures above 220 K. The fast diffusion of water suggests that heterogeneous ice nucleation on a glassy core is very unlikely in these systems. At temperatures below 220 K, model simulations of SOA droplets suggest that heterogeneous ice nucleation may occur in the immersion mode on glassy cores which remain embedded in a liquid shell when experiencing fast updraft velocities. The particles absorb significant quantities of water during these updrafts which plasticize their outer layers such that these layers equilibrate readily with the gas phase humidity before the homogeneous ice nucleation threshold is reached. Glass formation is thus unlikely to restrict homogeneous ice nucleation. Only under most extreme conditions near the very high tropical tropopause may the homogeneous ice nucleation rate coefficient be reduced as a consequence of slow condensed-phase water diffusion. Since the differences between the behavior limited or non limited by diffusion are small even at the very high tropical tropopause, condensed-phase water diffusivity is unlikely to have significant consequences on the direct climatic effects of SOA particles under tropospheric conditions.

scholarly journals Observation of viscosity transition in <i>α</i>-pinene secondary organic aerosol

2016 ◽  
Vol 16 (7) ◽  
pp. 4423-4438 ◽  
Author(s):  
Emma Järvinen ◽  
Karoliina Ignatius ◽  
Leonid Nichman ◽  
Thomas B. Kristensen ◽  
Claudia Fuchs ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Nuclear Research ◽  
Spherical Shape ◽  
Amorphous Solid ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Spherical Particles ◽  
Ambient Conditions ◽  
Wide Range ◽  
Viscous State

Abstract. Under certain conditions, secondary organic aerosol (SOA) particles can exist in the atmosphere in an amorphous solid or semi-solid state. To determine their relevance to processes such as ice nucleation or chemistry occurring within particles requires knowledge of the temperature and relative humidity (RH) range for SOA to exist in these states. In the Cosmics Leaving Outdoor Droplets (CLOUD) experiment at The European Organisation for Nuclear Research (CERN), we deployed a new in situ optical method to detect the viscous state of α-pinene SOA particles and measured their transition from the amorphous highly viscous state to states of lower viscosity. The method is based on the depolarising properties of laboratory-produced non-spherical SOA particles and their transformation to non-depolarising spherical particles at relative humidities near the deliquescence point. We found that particles formed and grown in the chamber developed an asymmetric shape through coagulation. A transition to a spherical shape was observed as the RH was increased to between 35 % at −10 °C and 80 % at −38 °C, confirming previous calculations of the viscosity-transition conditions. Consequently, α-pinene SOA particles exist in a viscous state over a wide range of ambient conditions, including the cirrus region of the free troposphere. This has implications for the physical, chemical, and ice-nucleation properties of SOA and SOA-coated particles in the atmosphere.

scholarly journals The effects of morphology, mobility size, and secondary organic aerosol (SOA) material coating on the ice nucleation activity of black carbon in the cirrus regime

2020 ◽  
Vol 20 (22) ◽  
pp. 13957-13984
Author(s):  
Cuiqi Zhang ◽  
Yue Zhang ◽  
Martin J. Wolf ◽  
Leonid Nichman ◽  
Chuanyang Shen ◽  
...  
Keyword(s):  
Black Carbon ◽  
State Transition ◽  
Phase State ◽  
Secondary Organic Aerosol ◽  
Global Climate ◽  
Surface Oxidation ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Supersaturation Ratio ◽  
Homogeneous Freezing

Abstract. There is evidence that black carbon (BC) particles may affect cirrus formation and, hence, global climate by acting as potential ice nucleating particles (INPs) in the troposphere. Nevertheless, the ice nucleation (IN) ability of bare BC and BC coated with secondary organic aerosol (SOA) material remains uncertain. We have systematically examined the IN ability of 100–400 nm size-selected BC particles with different morphologies and different SOA coatings representative of anthropogenic (toluene and n-dodecane) and biogenic (β-caryophyllene) sources in the cirrus regime (−46 to −38 ∘C). Several BC proxies were selected to represent different particle morphologies and oxidation levels. Atmospheric aging was further replicated with the exposure of SOA-coated BC to OH. The results demonstrate that the 400 nm hydrophobic BC types nucleate ice only at or near the homogeneous freezing threshold. Ice formation at cirrus temperatures below homogeneous freezing thresholds, as opposed to purely homogeneous freezing, was observed to occur for some BC types between 100 and 200 nm within the investigated temperature range. More fractal BC particles did not consistently act as superior INPs over more spherical ones. SOA coating generated by oxidizing β-caryophyllene with O3 did not seem to affect BC IN ability, probably due to an SOA-phase state transition. However, SOA coatings generated from OH oxidation of various organic species did exhibit higher IN-onset supersaturation ratio with respect to ice (SSi), compared with bare BC particles, with the toluene-SOA coating showing an increase in SSi of 0.1–0.15 while still below the homogeneous freezing threshold. Slightly oxidized toluene SOA coating seemed to have a stronger deactivation effect on BC IN ability than highly oxidized toluene SOA, which might be caused by oligomer formation and the phase state transition of toluene SOA under different oxidation levels. n-dodecane and β-caryophyllene-derived SOA-coated BC only froze in the homogeneous regime. We attribute the inhibition of IN ability to the filling of the pores on the BC surface by the SOA material coating. OH exposure levels of n-dodecane and β-caryophyllene SOA coating experiments, from an equivalent atmospheric exposure time from 10 to 90 d, did not render significant differences in the IN potential. Our study of selected BC types and sizes suggests that increases in diameter, compactness, and/or surface oxidation of BC particles lead to more efficient IN via the pore condensation freezing (PCF) pathway, and that coatings of common SOA materials can inhibit the formation of ice.

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.

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